Package 70518-1443-2

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1443-2
Digits Only 7051814432
Product NDC 70518-1443
Product ID 70518-1443_49008834-1b1f-9a67-e063-6394a90a10fa
Description

50 POUCH in 1 BOX (70518-1443-2) / 1 CAPSULE in 1 POUCH (70518-1443-3)

Marketing

Marketing Status
Marketed Since 2020-01-31
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": "49008834-1b1f-9a67-e063-6394a90a10fa", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141"], "spl_set_id": ["39e3fa5d-ea48-4b02-80f6-44591f5e013f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "50 POUCH in 1 BOX (70518-1443-2)  / 1 CAPSULE in 1 POUCH (70518-1443-3)", "package_ndc": "70518-1443-2", "marketing_start_date": "20200131"}], "brand_name": "Prazosin Hydrochloride", "product_id": "70518-1443_49008834-1b1f-9a67-e063-6394a90a10fa", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "70518-1443", "generic_name": "prazosin hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA072575", "marketing_category": "ANDA", "marketing_start_date": "20180928", "listing_expiration_date": "20271231"}