Package 37835-165-50

Brand: famotidine

Generic: famotidine
NDC Package

Package Facts

Identity

Package NDC 37835-165-50
Digits Only 3783516550
Product NDC 37835-165
Description

50 TABLET in 1 BOTTLE (37835-165-50)

Marketing

Marketing Status
Marketed Since 2025-06-01
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": "37e78f4b-58fb-8c28-e063-6294a90ad0b0", "openfda": {"nui": ["N0000000151", "N0000175784"], "unii": ["5QZO15J2Z8"], "rxcui": ["310273"], "spl_set_id": ["140440fb-d420-490d-8d7d-4b01c8ed3a83"], "pharm_class_epc": ["Histamine-2 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Histamine H2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Bi-Mart"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (37835-165-50)", "package_ndc": "37835-165-50", "marketing_start_date": "20250601"}], "brand_name": "Famotidine", "product_id": "37835-165_37e78f4b-58fb-8c28-e063-6294a90ad0b0", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "37835-165", "generic_name": "Famotidine", "labeler_name": "Bi-Mart", "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": "20250601", "listing_expiration_date": "20261231"}