Package 43063-260-30

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-260-30
Digits Only 4306326030
Product NDC 43063-260
Product ID 43063-260_41acdd32-11a7-fe53-e063-6394a90a3623
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (43063-260-30)

Marketing

Marketing Status
Marketed Since 2010-06-23
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": "41acdd32-11a7-fe53-e063-6394a90a3623", "openfda": {"upc": ["0343063260302"], "unii": ["X0Z7454B90"], "rxcui": ["312594"], "spl_set_id": ["cd52f022-ca29-4f87-8684-da63e05b3c1f"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (43063-260-30)", "package_ndc": "43063-260-30", "marketing_start_date": "20100623"}], "brand_name": "Prazosin Hydrochloride", "product_id": "43063-260_41acdd32-11a7-fe53-e063-6394a90a3623", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "43063-260", "generic_name": "prazosin hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA072575", "marketing_category": "ANDA", "marketing_start_date": "19890228", "listing_expiration_date": "20261231"}