Package 0172-5728-60

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 0172-5728-60
Digits Only 0172572860
Product NDC 0172-5728
Description

100 TABLET, FILM COATED in 1 BOTTLE (0172-5728-60)

Marketing

Marketing Status
Marketed Since 2001-04-16
Brand famotidine
Generic famotidine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4f26d0af-7f08-49a1-8bba-46741aa83ad5", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245", "310273"], "spl_set_id": ["4c6f4f9e-f3f5-4ecf-9f40-887e037e8847"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0172-5728-60)", "package_ndc": "0172-5728-60", "marketing_start_date": "20010416"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (0172-5728-70)", "package_ndc": "0172-5728-70", "marketing_start_date": "20010416"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (0172-5728-80)", "package_ndc": "0172-5728-80", "marketing_start_date": "20010416"}], "brand_name": "Famotidine", "product_id": "0172-5728_4f26d0af-7f08-49a1-8bba-46741aa83ad5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "0172-5728", "generic_name": "Famotidine", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA075511", "marketing_category": "ANDA", "marketing_start_date": "20010416", "listing_expiration_date": "20261231"}