Generated automatically from the NAFDAC register, WHO alerts and community data as of today. Not medical advice — always follow your doctor or pharmacist.
From the official U.S. FDA label for rabies vaccine (inactivated), the active ingredient registered with NAFDAC.
Temporarily relieves symptoms of runny nose, fever & cough.**
Temporarily relieves symptoms of runny nose, fever & cough.**
IF PREGNANT OR BREAST-FEEDING , ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. Do not use if TAMPER EVIDENT seal is broken or missing.
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Nobivac Rabies (1 dose) contains Rabies vaccine (inactivated) (see Composition), as suspension for injection, according to its NAFDAC registration record.
Yes. Nobivac Rabies (1 dose) is listed on the NAFDAC register under registration number 04-3251, and its registration is active as of 5 November 2026.
No WHO falsified or substandard medical product alert currently matches Nobivac Rabies (1 dose) in our automatically synced alert list.
Run a free authenticity scan with the NAFDAC number 04-3251, 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.
Temporarily relieves symptoms of runny nose, fever & cough.** (Summarised from the official U.S. FDA label for rabies vaccine (inactivated). Always follow your doctor or pharmacist.)
Reviews are personal experiences from RxVerify users, not medical advice. Report side effects to your doctor and to NAFDAC.