Package 68180-150-01
Brand: famotidine
Generic: famotidinePackage Facts
Identity
Package NDC
68180-150-01
Digits Only
6818015001
Product NDC
68180-150
Description
50 mL in 1 BOTTLE (68180-150-01)
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": "ce0e39ea-0d29-4922-95cb-8777326a994e", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0368180150015"], "unii": ["5QZO15J2Z8"], "rxcui": ["310274"], "spl_set_id": ["2caaf94b-b382-4573-8614-57815776b659"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (68180-150-01)", "package_ndc": "68180-150-01", "marketing_start_date": "20100629"}], "brand_name": "Famotidine", "product_id": "68180-150_ce0e39ea-0d29-4922-95cb-8777326a994e", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "68180-150", "generic_name": "Famotidine", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Famotidine", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/5mL"}], "application_number": "ANDA090440", "marketing_category": "ANDA", "marketing_start_date": "20100629", "listing_expiration_date": "20261231"}