Package 70377-067-11

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70377-067-11
Digits Only 7037706711
Product NDC 70377-067
Product ID 70377-067_99deacbe-59a1-4e72-8b23-d0f470e2633d
Description

100 CAPSULE in 1 BOTTLE (70377-067-11)

Marketing

Marketing Status
Marketed Since 2023-01-09
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": "99deacbe-59a1-4e72-8b23-d0f470e2633d", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141", "312593", "312594"], "spl_set_id": ["82a84f69-4742-453f-96c8-532fb7df44c6"], "manufacturer_name": ["Biocon Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (70377-067-11)", "package_ndc": "70377-067-11", "marketing_start_date": "20230109"}], "brand_name": "Prazosin hydrochloride", "product_id": "70377-067_99deacbe-59a1-4e72-8b23-d0f470e2633d", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "70377-067", "generic_name": "Prazosin hydrochloride", "labeler_name": "Biocon Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA213406", "marketing_category": "ANDA", "marketing_start_date": "20230109", "listing_expiration_date": "20261231"}