Package 58602-829-34
Brand: famotidine
Generic: famotidinePackage Facts
Identity
Package NDC
58602-829-34
Digits Only
5860282934
Product NDC
58602-829
Description
1 BOTTLE in 1 CARTON (58602-829-34) / 200 TABLET, FILM COATED in 1 BOTTLE
Marketing
Marketing Status
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": "d4587b3e-852f-49b4-8237-1cd6e20e063a", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["5b161f25-c578-4ff4-a931-ff3a1e681c50"], "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 (58602-829-21) / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-829-21", "marketing_start_date": "20160426"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-829-34) / 200 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-829-34", "marketing_start_date": "20210325"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-829-50) / 85 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "58602-829-50", "marketing_start_date": "20210302"}], "brand_name": "Famotidine", "product_id": "58602-829_d4587b3e-852f-49b4-8237-1cd6e20e063a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "58602-829", "generic_name": "Famotidine", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA206531", "marketing_category": "ANDA", "marketing_start_date": "20160426", "listing_expiration_date": "20261231"}