Package 64980-636-03

Brand: ranitidine

Generic: ranitidine
NDC Package

Package Facts

Identity

Package NDC 64980-636-03
Digits Only 6498063603
Product NDC 64980-636
Product ID 64980-636_b4d3aa30-82b1-45e5-89bb-829c5ccf7ffe
Description

30 TABLET in 1 BOTTLE (64980-636-03)

Marketing

Marketing Status
Marketed Since 2025-12-06
Brand ranitidine
Generic ranitidine
Sample Package No

Linked Drug Pages (1)

RANITIDINE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b4d3aa30-82b1-45e5-89bb-829c5ccf7ffe", "openfda": {"upc": ["0364980637039"], "unii": ["BK76465IHM"], "rxcui": ["198191", "198193"], "spl_set_id": ["0fba6615-37c2-4ba6-b6e5-09599369a5bc"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (64980-636-03)", "package_ndc": "64980-636-03", "marketing_start_date": "20251206"}], "brand_name": "RANITIDINE", "product_id": "64980-636_b4d3aa30-82b1-45e5-89bb-829c5ccf7ffe", "dosage_form": "TABLET", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "64980-636", "generic_name": "RANITIDINE", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RANITIDINE", "active_ingredients": [{"name": "RANITIDINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA211289", "marketing_category": "ANDA", "marketing_start_date": "20251206", "listing_expiration_date": "20261231"}