Package 70518-3271-0

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3271-0
Digits Only 7051832710
Product NDC 70518-3271
Product ID 70518-3271_3a3a091d-7364-59a7-e063-6294a90a5fca
Description

30 POUCH in 1 BOX (70518-3271-0) / 1 CAPSULE in 1 POUCH (70518-3271-1)

Marketing

Marketing Status
Marketed Since 2021-11-17
Brand prazosin hydrochloride
Generic prazosin hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3a3a091d-7364-59a7-e063-6294a90a5fca", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["312593"], "spl_set_id": ["2f86fc8e-71c1-4749-b67e-86d86cf1d984"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 BOX (70518-3271-0)  / 1 CAPSULE in 1 POUCH (70518-3271-1)", "package_ndc": "70518-3271-0", "marketing_start_date": "20211117"}], "brand_name": "Prazosin Hydrochloride", "product_id": "70518-3271_3a3a091d-7364-59a7-e063-6294a90a5fca", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3271", "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": "NDA017442", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20211117", "listing_expiration_date": "20261231"}