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Hydralazine Injection

NAFDAC Reg. No. B4-9061 · Drug

Registered with NAFDAC — registration activeAs of 5 November 2026 · synced automatically from official sources.
Product
Hydralazine Injection
NAFDAC number
B4-9061
Active ingredient
Hydralazine Hydrochloride
Strength
20 mg/mL
Form
Solution for injection
Pack size
1 mL x 10's (in amber coloured ampoules)
Manufacturer
Not listed
Applicant (holder)
Chez Resources Pharmaceutical Limited
Approved
28 Feb 2024
Status
Active View on NAFDAC ↗
Registration valid to
27 Feb 2029
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • Hydralazine Injection is on the NAFDAC register with an active registration (B4-9061). 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 Hydralazine Injection is used for

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

What it is used for

Essential hypertension, alone or as an adjunct.

Possible side effects

Adverse reactions with hydrALAZINE are usually reversible when dosage is reduced. However, in some cases it may be necessary to discontinue the drug. The following adverse reactions have been observed, but there has not been enough systematic collection of data to support an estimate of their frequency. Common Headache, anorexia, nausea, vomiting, diarrhea, palpitations, tachycardia, angina pectoris. Less Frequent: Digestive: constipation, paralytic ileus. Cardiovascular: hypotension, paradoxical pressor response, edema. Respiratory: dyspnea. …

Do not use if

Hypersensitivity to hydrALAZINE; coronary artery disease; mitral valvular rheumatic heart disease.

Warnings

​ In a few patients hydrALAZINE may produce a clinical picture simulating systemic lupus erythematosus including glomerulonephritis. In such patients hydrALAZINE should be discontinued unless the benefit-to-risk determination requires continued antihypertensive therapy with this drug. Symptoms and signs usually regress when the drug is discontinued but residua have been detected many years later. Long-term treatment with steroids may be necessary. (See PRECAUTIONS, Laboratory Tests .)

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

Check your pack of Hydralazine 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 Hydralazine Injection

What is in Hydralazine Injection?

Hydralazine Injection contains Hydralazine Hydrochloride (20 mg/mL), as solution for injection, according to its NAFDAC registration record.

Is Hydralazine Injection registered with NAFDAC?

Yes. Hydralazine Injection is listed on the NAFDAC register under registration number B4-9061, and its registration is active as of 5 November 2026.

Has Hydralazine Injection been flagged as fake or recalled?

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

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

Run a free authenticity scan with the NAFDAC number B4-9061, 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 Hydralazine Injection used for?

Essential hypertension, alone or as an adjunct. (Summarised from the official U.S. FDA label for hydralazine 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.