Package 21130-191-20
Brand: famotidine
Generic: famotidinePackage Facts
Identity
Package NDC
21130-191-20
Digits Only
2113019120
Product NDC
21130-191
Description
200 TABLET in 1 BOTTLE (21130-191-20)
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": "463f1b83-03cb-ec46-e063-6294a90a7168", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["f18c1195-48a1-69dc-e053-2a95a90a4077"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["SAFEWAY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (21130-191-20)", "package_ndc": "21130-191-20", "marketing_start_date": "20230630"}], "brand_name": "Famotidine", "product_id": "21130-191_463f1b83-03cb-ec46-e063-6294a90a7168", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "21130-191", "generic_name": "Famotidine", "labeler_name": "SAFEWAY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "20 mg/1"}], "application_number": "ANDA215822", "marketing_category": "ANDA", "marketing_start_date": "20230630", "listing_expiration_date": "20261231"}