NDC 68788-8742 – Prazosin Hydrochloride

Prazosin Hydrochloride 2 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC68788-8742

Product details

Brand name
Prazosin Hydrochloride
Generic name
Prazosin Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA210971
Marketed since
September 23, 2024
Listing expires
December 31, 2027
Pharmacologic class
alpha-Adrenergic Blocker

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
68788-8742-1100 CAPSULE in 1 BOTTLE (68788-8742-1)Sep 23, 2024
68788-8742-330 CAPSULE in 1 BOTTLE (68788-8742-3)Sep 23, 2024
68788-8742-660 CAPSULE in 1 BOTTLE (68788-8742-6)Sep 23, 2024
68788-8742-990 CAPSULE in 1 BOTTLE (68788-8742-9)Sep 23, 2024

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