Package 0121-1025-08

Brand: cimetidine hydrochloride

Generic: cimetidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0121-1025-08
Digits Only 0121102508
Product NDC 0121-1025
Product ID 0121-1025_55abdac4-2b7c-4163-bf5f-d2e934108ba6
Description

237 mL in 1 BOTTLE (0121-1025-08)

Marketing

Marketing Status
Marketed Since 2025-01-09
Brand cimetidine hydrochloride
Generic cimetidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Cimetidine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "55abdac4-2b7c-4163-bf5f-d2e934108ba6", "openfda": {"upc": ["0301211025081"], "unii": ["WF10491673"], "rxcui": ["212787"], "spl_set_id": ["b8b50bd9-bc1b-4da5-96c5-8eb917c8937f"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (0121-1025-08)", "package_ndc": "0121-1025-08", "marketing_start_date": "20250109"}], "brand_name": "Cimetidine Hydrochloride", "product_id": "0121-1025_55abdac4-2b7c-4163-bf5f-d2e934108ba6", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "0121-1025", "generic_name": "Cimetidine Hydrochloride", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cimetidine Hydrochloride", "active_ingredients": [{"name": "CIMETIDINE HYDROCHLORIDE", "strength": "300 mg/5mL"}], "application_number": "ANDA074664", "marketing_category": "ANDA", "marketing_start_date": "20250109", "listing_expiration_date": "20261231"}