Package 76420-679-01

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76420-679-01
Digits Only 7642067901
Product NDC 76420-679
Description

100 TABLET in 1 BOTTLE (76420-679-01)

Marketing

Marketing Status
Marketed Since 2024-02-26
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": "1244caf6-4af2-dd22-e063-6294a90a81bd", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992438", "992447", "992475"], "spl_set_id": ["b4985d9d-1aa0-4b36-bc98-6a5410ad9bad"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-679-01)", "package_ndc": "76420-679-01", "marketing_start_date": "20240226"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-679-30)", "package_ndc": "76420-679-30", "marketing_start_date": "20240226"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-679-60)", "package_ndc": "76420-679-60", "marketing_start_date": "20240226"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-679-90)", "package_ndc": "76420-679-90", "marketing_start_date": "20240226"}], "brand_name": "Promethazine Hydrochloride", "product_id": "76420-679_1244caf6-4af2-dd22-e063-6294a90a81bd", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "76420-679", "generic_name": "Promethazine Hydrochloride", "labeler_name": "Asclemed USA, 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": "20051214", "listing_expiration_date": "20261231"}