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Anytidine Injection

NAFDAC Reg. No. A4-6769 · Drug

Registered with NAFDAC — registration activeAs of 5 November 2026 · synced automatically from official sources.
Product
Anytidine Injection
NAFDAC number
A4-6769
Active ingredient
Ranitidine (Ranitidine Hydrochloride)
Strength
50 mg/2 mL
Form
Injection
Pack size
5 x 2 mL (in amber glass ampoules)
Manufacturer
Not listed
Applicant (holder)
Amakin Pharmaceuticals Nigeria Limited
Approved
22 Oct 2022
Status
Active View on NAFDAC ↗
Registration valid to
21 Oct 2027
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • Anytidine Injection is on the NAFDAC register with an active registration (A4-6769). 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 Anytidine Injection is used for

From the official U.S. FDA label for ranitidine (ranitidine hydrochloride), the active ingredient registered with NAFDAC.

What it is used for

(s) relieves heartburn associated with acid indigestion and sour stomach prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages

Purpose

Acid reducer

Possible side effects

Stop use and ask doctor if your heartburn continues or worsens you need to take this product for more than 14 days

Do not use if

if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools.These may be signs of a serious condition. See your doctor. with other acid reducers

Warnings

Allergy alert: Do not use if you are allergic to ranitidine or other acid reducers Do not use if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools.These may be signs of a serious condition. See your doctor. with other acid reducers Ask a doctor before use if you have had heartburn over 3 months. This may be a sign of a more serious condition. …

Pregnancy & breastfeeding

If pregnant or breast-feeding, ask a health professional before use.

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

Check your pack of Anytidine Injection

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 Anytidine Injection

What is in Anytidine Injection?

Anytidine Injection contains Ranitidine (Ranitidine Hydrochloride) (50 mg/2 mL), as injection, according to its NAFDAC registration record.

Is Anytidine Injection registered with NAFDAC?

Yes. Anytidine Injection is listed on the NAFDAC register under registration number A4-6769, and its registration is active as of 5 November 2026.

Has Anytidine Injection been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Anytidine Injection in our automatically synced alert list.

How can I check that my pack of Anytidine Injection is genuine?

Run a free authenticity scan with the NAFDAC number A4-6769, 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 Anytidine Injection used for?

(s) relieves heartburn associated with acid indigestion and sour stomach prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages (Summarised from the official U.S. FDA label for ranitidine (ranitidine hydrochloride). Always follow your doctor or pharmacist.)

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Reviews are personal experiences from RxVerify users, not medical advice. Report side effects to your doctor and to NAFDAC.