Package 68999-809-24

Brand: cimetidine hydrochloride

Generic: cimetidine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68999-809-24
Digits Only 6899980924
Product NDC 68999-809
Description

2 TRAY in 1 BOX (68999-809-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-809-05)

Marketing

Marketing Status
Marketed Since 2025-10-23
Brand cimetidine hydrochloride
Generic cimetidine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "42c607ee-eb27-a72c-e063-6394a90a653c", "openfda": {"unii": ["WF10491673"], "rxcui": ["212787"], "spl_set_id": ["e40bb1f6-338a-42e7-9217-8c32d14ccfd3"], "manufacturer_name": ["Chartwell Governmental & Specialty RX, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TRAY in 1 BOX (68999-809-24)  / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-809-05)", "package_ndc": "68999-809-24", "marketing_start_date": "20251023"}], "brand_name": "CIMETIDINE HYDROCHLORIDE", "product_id": "68999-809_42c607ee-eb27-a72c-e063-6394a90a653c", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H2 Receptor Antagonists [MoA]", "Histamine-2 Receptor Antagonist [EPC]"], "product_ndc": "68999-809", "generic_name": "CIMETIDINE HYDROCHLORIDE", "labeler_name": "Chartwell Governmental & Specialty RX, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CIMETIDINE HYDROCHLORIDE", "active_ingredients": [{"name": "CIMETIDINE HYDROCHLORIDE", "strength": "300 mg/5mL"}], "application_number": "ANDA074251", "marketing_category": "ANDA", "marketing_start_date": "19941222", "listing_expiration_date": "20261231"}