Package 70518-3352-0

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3352-0
Digits Only 7051833520
Product NDC 70518-3352
Product ID 70518-3352_3a72c730-1c20-e2bf-e063-6294a90a3892
Description

100 POUCH in 1 BOX (70518-3352-0) / 1 CAPSULE in 1 POUCH (70518-3352-1)

Marketing

Marketing Status
Marketed Since 2022-01-31
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": "3a72c730-1c20-e2bf-e063-6294a90a3892", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141"], "spl_set_id": ["a3045d80-33f4-4aab-8dce-42fbbf9d3ef7"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-3352-0)  / 1 CAPSULE in 1 POUCH (70518-3352-1)", "package_ndc": "70518-3352-0", "marketing_start_date": "20220131"}], "brand_name": "Prazosin Hydrochloride", "product_id": "70518-3352_3a72c730-1c20-e2bf-e063-6294a90a3892", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3352", "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": "ANDA071745", "marketing_category": "ANDA", "marketing_start_date": "20220131", "listing_expiration_date": "20261231"}