Package 68071-2972-1

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-2972-1
Digits Only 6807129721
Product NDC 68071-2972
Description

100 CAPSULE in 1 BOTTLE (68071-2972-1)

Marketing

Marketing Status
Marketed Since 2023-04-10
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": "292cb35f-8034-23a8-e063-6294a90aef4c", "openfda": {"upc": ["0368071297218"], "unii": ["X0Z7454B90"], "rxcui": ["312594"], "spl_set_id": ["f8fd7e1d-471d-f4ae-e053-6294a90a8b41"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68071-2972-1)", "package_ndc": "68071-2972-1", "marketing_start_date": "20230410"}], "brand_name": "prazosin hydrochloride", "product_id": "68071-2972_292cb35f-8034-23a8-e063-6294a90aef4c", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "68071-2972", "generic_name": "prazosin hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prazosin hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA215697", "marketing_category": "ANDA", "marketing_start_date": "20230103", "listing_expiration_date": "20261231"}