Package 68001-161-00
Brand: promethazine hydrochloride
Generic: promethazine hydrochloridePackage Facts
Identity
Package NDC
68001-161-00
Digits Only
6800116100
Product NDC
68001-161
Description
100 TABLET in 1 BOTTLE (68001-161-00)
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": "3d817fa0-d0c1-9b87-e063-6394a90af502", "openfda": {"upc": ["0368001161008", "0368001162005", "0368001163002"], "unii": ["R61ZEH7I1I"], "rxcui": ["992438", "992447", "992475"], "spl_set_id": ["44cd6d46-fbb9-4836-9426-d8ce2cb6d66d"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68001-161-00)", "package_ndc": "68001-161-00", "marketing_start_date": "20140113"}], "brand_name": "Promethazine Hydrochloride", "product_id": "68001-161_3d817fa0-d0c1-9b87-e063-6394a90af502", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "68001-161", "generic_name": "Promethazine Hydrochloride", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA040596", "marketing_category": "ANDA", "marketing_start_date": "20140113", "listing_expiration_date": "20261231"}