Package 58602-828-19

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 58602-828-19
Digits Only 5860282819
Product NDC 58602-828
Description

1 BOTTLE in 1 CARTON (58602-828-19) / 90 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2016-04-26
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": "01351d50-0222-4f6c-93cc-66b2afb98669", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0358602828196"], "unii": ["5QZO15J2Z8"], "rxcui": ["199047"], "spl_set_id": ["27ecf5c1-202a-44cf-94f9-d7fefa027e1e"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-828-19)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-828-19", "marketing_start_date": "20160426"}], "brand_name": "Famotidine", "product_id": "58602-828_01351d50-0222-4f6c-93cc-66b2afb98669", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "58602-828", "generic_name": "Famotidine", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "10 mg/1"}], "application_number": "ANDA206531", "marketing_category": "ANDA", "marketing_start_date": "20160426", "listing_expiration_date": "20261231"}