Package 59651-701-50
Brand: famotidine
Generic: famotidinePackage Facts
Identity
Package NDC
59651-701-50
Digits Only
5965170150
Product NDC
59651-701
Description
50 mL in 1 BOTTLE (59651-701-50)
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": "186342b3-2a01-4582-8978-41f059d4307d", "openfda": {"nui": ["N0000000151", "N0000175784"], "upc": ["0359651701508"], "unii": ["5QZO15J2Z8"], "rxcui": ["310274"], "spl_set_id": ["18066b80-1ec6-4092-80d9-70adb0ecac85"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (59651-701-50)", "package_ndc": "59651-701-50", "marketing_start_date": "20250709"}], "brand_name": "FAMOTIDINE", "product_id": "59651-701_186342b3-2a01-4582-8978-41f059d4307d", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "59651-701", "generic_name": "FAMOTIDINE", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FAMOTIDINE", "active_ingredients": [{"name": "FAMOTIDINE", "strength": "40 mg/5mL"}], "application_number": "ANDA219091", "marketing_category": "ANDA", "marketing_start_date": "20250709", "listing_expiration_date": "20271231"}