Package 68788-7886-8

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-7886-8
Digits Only 6878878868
Product NDC 68788-7886
Description

12 TABLET in 1 BOTTLE (68788-7886-8)

Marketing

Marketing Status
Marketed Since 2021-04-16
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": "5c684bfa-9a87-4298-a8f3-407c841a764f", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992447"], "spl_set_id": ["974208c8-4aad-4fb9-991b-cf3085034272"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (68788-7886-1)", "package_ndc": "68788-7886-1", "marketing_start_date": "20210416"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-7886-2)", "package_ndc": "68788-7886-2", "marketing_start_date": "20210416"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7886-3)", "package_ndc": "68788-7886-3", "marketing_start_date": "20210416"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE (68788-7886-8)", "package_ndc": "68788-7886-8", "marketing_start_date": "20210416"}], "brand_name": "Promethazine Hydrochloride", "product_id": "68788-7886_5c684bfa-9a87-4298-a8f3-407c841a764f", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "68788-7886", "generic_name": "Promethazine Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20210416", "listing_expiration_date": "20261231"}