Package 70518-3679-0

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3679-0
Digits Only 7051836790
Product NDC 70518-3679
Product ID 70518-3679_468a9737-9b8d-ca54-e063-6394a90a7a8a
Description

30 CAPSULE in 1 BLISTER PACK (70518-3679-0)

Marketing

Marketing Status
Marketed Since 2023-03-12
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": "468a9737-9b8d-ca54-e063-6394a90a7a8a", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["312594"], "spl_set_id": ["8606d9b8-4529-4689-8c93-7114c84c2e54"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-3679-0)", "package_ndc": "70518-3679-0", "marketing_start_date": "20230312"}], "brand_name": "prazosin hydrochloride", "product_id": "70518-3679_468a9737-9b8d-ca54-e063-6394a90a7a8a", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3679", "generic_name": "prazosin hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20230312", "listing_expiration_date": "20261231"}