Package 71205-535-30

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 71205-535-30
Digits Only 7120553530
Product NDC 71205-535
Product ID 71205-535_37ca9d4f-3fed-421a-a18f-a9954c00a90c
Description

30 TABLET, FILM COATED in 1 BOTTLE (71205-535-30)

Marketing

Marketing Status
Marketed Since 2021-02-16
Brand famotidine
Generic famotidine
Sample Package No

Linked Drug Pages (1)

Famotidine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "37ca9d4f-3fed-421a-a18f-a9954c00a90c", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0371205535308"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["4adb4864-04ac-4cb1-96c2-6196a30ac640"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (71205-535-06)", "package_ndc": "71205-535-06", "marketing_start_date": "20210224"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71205-535-10)", "package_ndc": "71205-535-10", "marketing_start_date": "20210224"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-535-30)", "package_ndc": "71205-535-30", "marketing_start_date": "20210216"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-535-60)", "package_ndc": "71205-535-60", "marketing_start_date": "20210216"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71205-535-78)", "package_ndc": "71205-535-78", "marketing_start_date": "20240906"}], "brand_name": "Famotidine", "product_id": "71205-535_37ca9d4f-3fed-421a-a18f-a9954c00a90c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "71205-535", "generic_name": "Famotidine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA206530", "marketing_category": "ANDA", "marketing_start_date": "20151222", "listing_expiration_date": "20261231"}