Package 0904-7022-61

Brand: prazosin hydrochloride

Generic: prazosin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7022-61
Digits Only 0904702261
Product NDC 0904-7022
Product ID 0904-7022_693144cc-ea54-4a3d-9938-9b4051a64f0b
Description

100 BLISTER PACK in 1 CARTON (0904-7022-61) / 1 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2018-10-03
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": "693144cc-ea54-4a3d-9938-9b4051a64f0b", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141", "312593", "312594"], "spl_set_id": ["4f55f4db-dab3-4e50-9f71-5595fd3ccc12"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7022-61)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7022-61", "marketing_start_date": "20181003"}], "brand_name": "Prazosin Hydrochloride", "product_id": "0904-7022_693144cc-ea54-4a3d-9938-9b4051a64f0b", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "0904-7022", "generic_name": "Prazosin Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA210971", "marketing_category": "ANDA", "marketing_start_date": "20181003", "listing_expiration_date": "20271231"}