Package 60760-821-30

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-821-30
Digits Only 6076082130
Product NDC 60760-821
Product ID 60760-821_35a9c719-ffbd-e02a-e063-6294a90a05c7
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (60760-821-30)

Marketing

Marketing Status
Marketed Since 2025-05-13
Brand prazosin hydrochloride
Generic prazosin hydrochloride
Sample Package No

Linked Drug Pages (1)

prazosin hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "35a9c719-ffbd-e02a-e063-6294a90a05c7", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["312594"], "spl_set_id": ["35a9c70d-b611-cf9d-e063-6294a90a23f7"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (60760-821-30)", "package_ndc": "60760-821-30", "marketing_start_date": "20250513"}], "brand_name": "prazosin hydrochloride", "product_id": "60760-821_35a9c719-ffbd-e02a-e063-6294a90a05c7", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "60760-821", "generic_name": "prazosin hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prazosin hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA215697", "marketing_category": "ANDA", "marketing_start_date": "20230103", "listing_expiration_date": "20261231"}