Package 70518-4489-0

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4489-0
Digits Only 7051844890
Product NDC 70518-4489
Description

30 CAPSULE in 1 BLISTER PACK (70518-4489-0)

Marketing

Marketing Status
Marketed Since 2025-10-01
Brand prazosin hydrochloride
Generic prazosin hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "401b35fc-bb65-2851-e063-6394a90a2306", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["312593"], "spl_set_id": ["2aa62e0a-442d-41af-a2d8-0b8f88d23319"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4489-0)", "package_ndc": "70518-4489-0", "marketing_start_date": "20251001"}], "brand_name": "Prazosin Hydrochloride", "product_id": "70518-4489_401b35fc-bb65-2851-e063-6394a90a2306", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "70518-4489", "generic_name": "Prazosin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA213052", "marketing_category": "ANDA", "marketing_start_date": "20251001", "listing_expiration_date": "20261231"}