सत्यापित हो रहा है..
स्वचालित रूप से अनुवादित। खुराक और चेतावनियाँ: मूल अंग्रेज़ी में देखें। अंग्रेज़ी में पढ़ें

Anytidine Injection

NAFDAC Reg. No. A4-6769 · दवा

NAFDAC के साथ रजिस्टर किया गया। रजिस्ट्रेशन ऐक्टिव हैAs of 29 October 2026 · synced automatically from official sources.
उत्पाद
Anytidine Injection
NAFDAC नंबर
A4-6769
सक्रिय घटक
Ranitidine (Ranitidine Hydrochloride)
प्रबलता
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

About the medicine: Ranitidine: uses, dosage and brands worldwide

What we found

  • 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. This is not medical advice. Always follow your doctor or pharmacist.

How to use Anytidine Injection

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

यह किसके लिए है

(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

How to take it and how often
  • Adults and children 12 years and over: to relieve symptoms, swallow 1 tablet with a glass of water to prevent symptoms, swallow 1 tablet with a glass of water 30 to 60 minutes before eating food or drinking beverages that cause heartburn can be used up to twice daily (do not take more than 2 tablets in 24 hours)
  • Children under 12 years: ask a doctor
Talk to a doctor first if
  • Had heartburn over 3 months
  • This may be a sign of a more serious condition. heartburn with lightheadedness, sweating or dizziness chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness frequent chest pain frequent wheezing, particularly with heartburn unexplained weight loss nausea or vomiting stomach pain kidney disease
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. …

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

Pregnancy and breastfeeding

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

How to store it

Keep out of reach of children.

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2025-05-23.

Label for ranitidine (ranitidine hydrochloride), the active ingredient registered with NAFDAC.

Check your pack of Anytidine Injection

Add the expiry date on your pack for a full Trust Score.

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

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 29 October 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.

How do I take Anytidine Injection?

Follow your prescription or the leaflet in your pack. The official label says: adults and children 12 years and over: to relieve symptoms, swallow 1 tablet with a glass of water to prevent symptoms, swallow 1 tablet with a glass of water 30 to 60 minutes before eating food or drinking beverages that cause heartburn can be used up to twice daily (do not take more than 2 tablets in 24 hours) children under 12 years: ask a doctor…

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.)

Patient reviews

–No reviews yet
5★
0
4★
0
3★
0
2★
0
1★
0
Have you used Anytidine Injection? Share your experience to help other patients. Sign in to review

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