Package 70518-2178-2

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-2178-2
Digits Only 7051821782
Product NDC 70518-2178
Product ID 70518-2178_49dae439-65b6-e69b-e063-6294a90a3992
Description

100 POUCH in 1 BOX (70518-2178-2) / 1 CAPSULE in 1 POUCH (70518-2178-3)

Marketing

Marketing Status
Marketed Since 2023-03-28
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": "49dae439-65b6-e69b-e063-6294a90a3992", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["312594"], "spl_set_id": ["4eaa58c1-a5c5-49b4-a8ac-89f12eb29222"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2178-2)  / 1 CAPSULE in 1 POUCH (70518-2178-3)", "package_ndc": "70518-2178-2", "marketing_start_date": "20230328"}], "brand_name": "Prazosin Hydrochloride", "product_id": "70518-2178_49dae439-65b6-e69b-e063-6294a90a3992", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "70518-2178", "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": "ANDA210971", "marketing_category": "ANDA", "marketing_start_date": "20190701", "listing_expiration_date": "20271231"}