Package 68001-162-00

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68001-162-00
Digits Only 6800116200
Product NDC 68001-162
Product ID 68001-162_3d817fa0-d0c1-9b87-e063-6394a90af502
Description

100 TABLET in 1 BOTTLE (68001-162-00)

Marketing

Marketing Status
Marketed Since 2014-01-13
Brand promethazine hydrochloride
Generic promethazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Promethazine Hydrochloride ndc-match (0.95)

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 (68001-162-00)", "package_ndc": "68001-162-00", "marketing_start_date": "20140113"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68001-162-03)", "package_ndc": "68001-162-03", "marketing_start_date": "20230727"}], "brand_name": "Promethazine Hydrochloride", "product_id": "68001-162_3d817fa0-d0c1-9b87-e063-6394a90af502", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "68001-162", "generic_name": "Promethazine Hydrochloride", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040596", "marketing_category": "ANDA", "marketing_start_date": "20140113", "listing_expiration_date": "20261231"}