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Vitamin K Tablets

NAFDAC Reg. No. C4-1152 · Drug

Registered with NAFDAC — registration activeAs of 6 November 2026 · synced automatically from official sources.
Product
Vitamin K Tablets
NAFDAC number
C4-1152
Active ingredient
Vitamin K3
Strength
10 mg
Form
Tablet
Manufacturer
Not listed
Applicant (holder)
Topsea Standard Pharmeceutical Company Ltd
Approved
10 Nov 2020
Status
Inactive View on NAFDAC ↗
Registration valid to
9 Nov 2025
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • Vitamin K Tablets is on the NAFDAC register with an active registration (C4-1152). 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 Vitamin K Tablets is used for

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

What it is used for

Multiple vitamins injection (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. Multiple vitamins injection (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 multiple vitamins injection (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

Multiple vitamins injection (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 Multiple vitamins injection (adult) contains aluminu …

Pregnancy & breastfeeding

8.1 Pregnancy Risk Summary Administration of the approved recommended dose of multiple vitamins injection (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. 023/2025 – Recall of Multivitamin Supplements due to Risk of Serious Injury or Death From Poisoning5 Jul 2025 · nafdac.gov.ngThe National Agency for Food and Drug Administration and Control (NAFDAC) is alerting the public about a recall of some batches of multivitamins and iron Supplements in the USA.These brands of vitamins, known as  CINCINNATI (WKRC), sold nationwide at retailers such as Walmart, Amazon, and Target, are being recalled due…Public Alert No. 0035/2022 – European Rapid Alert System For Dangerous Non-Food Products: Banned Cosmetic Product-Professional Mouse Pro-Vitamin B5 By United Kingdom Studio 2000 System21 Aug 2022 · nafdac.gov.ng, The National Agency for Food and Drug Administration and Control (NAFDAC)has received safety information from European Rapid Alert System for dangerous non- food products that a cosmetic product; Professional Mouse Pro-Vitamin B5 manufactured by United Kingdom Studio 2000 system has been banned. The product contains …Public Alert No. 0010/2021 – Falsified Vitamin A (Retinol) Identified In WHO Region of Africa7 Apr 2021 · nafdac.gov.ng, The National Agency for Food and Drugs Administration and Control (NAFDAC) has been notified by World Health Organization (WHO) on the circulation of two versions of falsified VITAMIN A (retinol) identified in Chad. Laboratory analysis of recovered samples revealed that both products are severely degraded and contain…Public Alert No. 0028/2018 – Recall Of Malco Vitamin B Complex Injection Manufactured By Shreechem Pharmaceuticals PVT. Limited13 Oct 2018 · nafdac.gov.ngThe National Agency for Food and Drug Administration and Control has been informed that the Zambia Medicines Regulatory Authority (ZARMA) has directed International Drug Company (IDC) Limited, Lusaka, Zambia to recall all batches of Malco (Vitamin B Complex) injection manufactured by Shreechem Pharmaceuticals PVT Limit…

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 Vitamin K 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 Vitamin K Tablets

What is in Vitamin K Tablets?

Vitamin K Tablets contains Vitamin K3 (10 mg), as tablet, according to its NAFDAC registration record.

Is Vitamin K Tablets registered with NAFDAC?

Yes. Vitamin K Tablets is listed on the NAFDAC register under registration number C4-1152, and its registration is active as of 6 November 2026.

Has Vitamin K Tablets been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Vitamin K Tablets in our automatically synced alert list.

How can I check that my pack of Vitamin K Tablets is genuine?

Run a free authenticity scan with the NAFDAC number C4-1152, 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 Vitamin K Tablets used for?

Multiple vitamins injection (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. Multiple vitamins injection (adult) is a combination of vitamins indicated for prevention (Summarised from the official U.S. FDA label for vitamin k. Always follow your doctor or pharmacist.)

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