Package 0904-7049-61

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 0904-7049-61
Digits Only 0904704961
Product NDC 0904-7049
Description

100 BLISTER PACK in 1 CARTON (0904-7049-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2010-10-04
Brand losartan potassium
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a343cef7-5a9d-43b9-adff-f27f6457fb2d", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["c15387df-87a4-4784-acb5-7dd550498f8f"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7049-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7049-61", "marketing_start_date": "20101004"}], "brand_name": "Losartan Potassium", "product_id": "0904-7049_a343cef7-5a9d-43b9-adff-f27f6457fb2d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "0904-7049", "generic_name": "Losartan Potassium", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA078243", "marketing_category": "ANDA", "marketing_start_date": "20101004", "listing_expiration_date": "20261231"}