NDC 68788-7335 – Prazosin Hydrochloride

Prazosin Hydrochloride 1 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC68788-7335

Product details

Brand name
Prazosin Hydrochloride
Generic name
Prazosin Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA071745
Marketed since
March 12, 2019
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
68788-7335-1100 CAPSULE in 1 BOTTLE (68788-7335-1)Mar 12, 2019
68788-7335-330 CAPSULE in 1 BOTTLE (68788-7335-3)Mar 12, 2019
68788-7335-660 CAPSULE in 1 BOTTLE (68788-7335-6)Mar 12, 2019
68788-7335-990 CAPSULE in 1 BOTTLE (68788-7335-9)Mar 12, 2019

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