Package 71335-2348-1

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2348-1
Digits Only 7133523481
Product NDC 71335-2348
Description

60 CAPSULE in 1 BOTTLE (71335-2348-1)

Marketing

Marketing Status
Marketed Since 2024-02-21
Brand prazosin hydrochloride
Generic prazosin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "154dc8f2-d0aa-40ed-9209-10428725aaa4", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141"], "spl_set_id": ["61e5108a-70eb-4d48-a742-defb2e918b63"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71335-2348-1)", "package_ndc": "71335-2348-1", "marketing_start_date": "20240221"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71335-2348-2)", "package_ndc": "71335-2348-2", "marketing_start_date": "20240221"}], "brand_name": "prazosin hydrochloride", "product_id": "71335-2348_154dc8f2-d0aa-40ed-9209-10428725aaa4", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2348", "generic_name": "prazosin hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prazosin hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA215697", "marketing_category": "ANDA", "marketing_start_date": "20230103", "listing_expiration_date": "20261231"}