Package 70518-3928-0

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3928-0
Digits Only 7051839280
Product NDC 70518-3928
Product ID 70518-3928_3bb15529-98fe-fc88-e063-6294a90a4a30
Description

30 CAPSULE in 1 BLISTER PACK (70518-3928-0)

Marketing

Marketing Status
Marketed Since 2023-11-29
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": "3bb15529-98fe-fc88-e063-6294a90a4a30", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["312593"], "spl_set_id": ["960f4d8d-6683-44ff-a3a7-e0f922e621b9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-3928-0)", "package_ndc": "70518-3928-0", "marketing_start_date": "20231129"}], "brand_name": "Prazosin hydrochloride", "product_id": "70518-3928_3bb15529-98fe-fc88-e063-6294a90a4a30", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3928", "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": "ANDA213406", "marketing_category": "ANDA", "marketing_start_date": "20231129", "listing_expiration_date": "20261231"}