NDC 60687-822 – Hydralazine Hydrochloride

Hydralazine Hydrochloride 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC60687-822

Product details

Brand name
Hydralazine Hydrochloride
Generic name
Hydralazine Hydrochloride
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040858
Marketed since
April 2, 2024
Listing expires
December 31, 2026
Pharmacologic class
Arteriolar Vasodilator

Active ingredients

Uses, dosage, side effects and warnings for Hydralazine Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
60687-822-01100 BLISTER PACK in 1 CARTON (60687-822-01) / 1 TABLET in 1 BLISTER PACK (60687-822-11)Apr 2, 2024

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