Package 67046-1447-3
Brand: promethazine hydrochloride
Generic: promethazine hydrochloridePackage Facts
Identity
Package NDC
67046-1447-3
Digits Only
6704614473
Product NDC
67046-1447
Description
30 TABLET in 1 BLISTER PACK (67046-1447-3)
Marketing
Marketing Status
Brand
promethazine hydrochloride
Generic
promethazine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d996626-a75c-950a-e063-6394a90a9c24", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992475"], "spl_set_id": ["2d996287-9eed-265a-e063-6294a90a6969"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1447-3)", "package_ndc": "67046-1447-3", "marketing_start_date": "20250207"}], "brand_name": "Promethazine Hydrochloride", "product_id": "67046-1447_2d996626-a75c-950a-e063-6394a90a9c24", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "67046-1447", "generic_name": "Promethazine Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040596", "marketing_category": "ANDA", "marketing_start_date": "20250207", "listing_expiration_date": "20261231"}