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Meta B-Fort Tablets_

NAFDAC Reg. No. A4-1872 · Drug

Registered with NAFDAC — registration activeAs of 6 November 2026 · synced automatically from official sources.
Product
Meta B-Fort Tablets_
NAFDAC number
A4-1872
Active ingredient
Vitamins
Strength
see Composition
Form
Tablet
Pack size
1 x 10's; 10 x 10's
Manufacturer
Not listed
Applicant (holder)
Vixa Pharmaceutical Company Limited
Approved
29 Mar 2021
Status
Inactive View on NAFDAC ↗
Registration valid to
28 Mar 2026
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • Meta B-Fort Tablets_ is on the NAFDAC register with an active registration (A4-1872). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. Not medical advice — always follow your doctor or pharmacist.

What Meta B-Fort Tablets_ is used for

From the official U.S. FDA label for vitamins, the active ingredient registered with NAFDAC.

What it is used for

INFUVITE ADULT is a combination of vitamins indicated for the prevention of vitamin deficiency in adults and children aged 11 and older receiving parenteral nutrition. The physician should not await the development of clinical signs of vitamin deficiency before initiating vitamin therapy. INFUVITE ADULT is a combination of vitamins indicated for prevention of vitamin deficiency in adults and children aged 11 and older receiving parenteral nutrition ( 1 )

Possible side effects

The following adverse reactions are discussed in greater detail in other section of the labeling. • Allergic reactions to thiamine [see Warnings and Precautions ( 5.2 )] • Hypervitaminosis A [see Warnings and Precautions ( 5.3 )] The following adverse reactions have been identified during postapproval use of INFUVITE ADULT. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. …

Do not use if

INFUVITE ADULT is contraindicated in patients who have • An existing hypervitaminosis, or • A history of hypersensitivity due to any vitamins or excipients contained in this formulation. • Hypersensitivity to any of the vitamins or excipients ( 4 ) • Existing hypervitaminosis ( 4 )

Warnings

• Risk of Aluminum Toxicity: For at risk patients (renal failure or those with prolonged therapy), consider periodic monitoring of aluminum levels ( 5.1 ) • Allergic Reactions: To thiamine may occur ( 5.2 ) • Hypervitaminosis A : Patients with renal failure or liver disease may be at higher risk ( 5.3 ) • Decreased Anticoagulant Effect of Warfarin: Monitor INR ( 5.4 , 7.1 ) • Interferes with Megaloblastic Anemia Diagnosis: Avoid during testing for this disorder ( 5.5 ) • Risk of Vitamin Deficiencies or Excesses: Monitor blood vitamin concentrations ( 5.6 ) • False Negative Urine Glucose Tests: Due to vitamin C ( 5.7 ) 5.1 Aluminum Toxicity INFUVITE ADULT contains aluminum that may be toxic. …

Pregnancy & breastfeeding

8.1 Pregnancy Risk Summary Administration of the approved recommended dose of INFUVITE ADULT in parental nutrition is not expected to cause major birth defects, miscarriage, or adverse maternal or fetal outcomes. Pregnant patients should follow the U.S. Recommended Daily Allowances for pregnancy because their vitamin requirements may exceed those of nonpregnant patients. …

General information only — not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

NAFDAC recall & alert notices

Public Alert No. 034/2026 – Niger Republic Imposes Import Ban on Bulmex Parboiled Rice from India due to Metallic Contamination12 Jul 2026 · nafdac.gov.ngThe National Agency for Food and Drug Administration and Control (NAFDAC) has been informed that the Niger Republic’s Ministry of Trade and Industry has banned the importation of Bulmex Parboiled Rice from India.The action was reportedly taken due to concerns raised during an investigation and regulatory oversight by t…Public Alert No.034/2022 – Mars Wrigley Confectionery US, LLC Issues Voluntary Recall of Specific Varieties of SKITTLES® Gummies, STARBURST® Gummies, and LIFE SAVERS® Gummies Due to Potential Presence of Thin Metal Strand Embedded in Gummies or Loose in the Bag3 Jun 2022 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control is notifying the public that Mars Wrigley Confectionery US, LLC announced a voluntary recall of specific varieties of SKITTLES® Gummies, STARBURST® Gummies, and LIFE SAVERS® Gummies. The recall was due to the potential presence of a very thin metal stra…Public Alert No. 035/2020 – On The Use Of Face Mask Containing Metal Parts During MRI Exams18 Dec 2020 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control has been informed by U.S Food and Drug Administration MedWatch that patients may be injured if they wear face masks with metal parts and coating during a Magnetic Resonance Imaging (MRI) exam. Metal parts like nose pieces sometimes called nose clips or …Public Alert No: 0012/2018 – Health Authority Orders The Withdrawal Of Metanor Flupirtine Capsule16 Jul 2018 · nafdac.gov.ngThe National Agency for Food and Drug Administration and Control (NAFDAC) has been informed that Portuguese Authority for Medicines and Health Product (INFARMED) on 1st April 2018 in Lisbon ordered the withdrawal of Mentanor, Flupirtine capsule 100 milligram because its active ingredient (Flupirtine) is harmful to the …

Notices list affected brands and batch numbers — compare them with your pack. Enter your batch number above to check it automatically.

Check your pack of Meta B-Fort Tablets_

Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.

3 free checks left today · no signup Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Meta B-Fort Tablets_

What is in Meta B-Fort Tablets_?

Meta B-Fort Tablets_ contains Vitamins (see Composition), as tablet, according to its NAFDAC registration record.

Is Meta B-Fort Tablets_ registered with NAFDAC?

Yes. Meta B-Fort Tablets_ is listed on the NAFDAC register under registration number A4-1872, and its registration is active as of 6 November 2026.

Has Meta B-Fort Tablets_ been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Meta B-Fort Tablets_ in our automatically synced alert list.

How can I check that my pack of Meta B-Fort Tablets_ is genuine?

Run a free authenticity scan with the NAFDAC number A4-1872, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

What is Meta B-Fort Tablets_ used for?

INFUVITE ADULT is a combination of vitamins indicated for the prevention of vitamin deficiency in adults and children aged 11 and older receiving parenteral nutrition. The physician should not await the development of clinical signs of vitamin deficiency before initiating vitamin therapy. INFUVITE ADULT is a combination of vitamins indicated for prevention of vitamin deficiency in adults and child (Summarised from the official U.S. FDA label for vitamins. Always follow your doctor or pharmacist.)

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