Package 43063-533-30
Brand: famotidine
Generic: famotidinePackage Facts
Identity
Package NDC
43063-533-30
Digits Only
4306353330
Product NDC
43063-533
Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-533-30)
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": "41392bae-3ede-5191-e063-6294a90ac386", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0343063533307"], "unii": ["5QZO15J2Z8"], "rxcui": ["284245"], "spl_set_id": ["5798d282-ce83-49aa-bc33-13203f2b5285"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-533-30)", "package_ndc": "43063-533-30", "marketing_start_date": "20140414"}], "brand_name": "Famotidine", "product_id": "43063-533_41392bae-3ede-5191-e063-6294a90ac386", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "43063-533", "generic_name": "Famotidine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/1"}], "application_number": "ANDA075511", "marketing_category": "ANDA", "marketing_start_date": "20010416", "listing_expiration_date": "20261231"}