Package 76420-389-30

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76420-389-30
Digits Only 7642038930
Product NDC 76420-389
Product ID 76420-389_36f60cbe-813d-cfa8-e063-6294a90a0b0a
Description

12 BLISTER PACK in 1 CARTON (76420-389-30) / 1 SUPPOSITORY in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-06-07
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": ["RECTAL"], "spl_id": "36f60cbe-813d-cfa8-e063-6294a90a0b0a", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992441", "992454"], "spl_set_id": ["1b1cee64-c0b5-4da6-92d0-1769350a5181"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "12 BLISTER PACK in 1 CARTON (76420-389-30)  / 1 SUPPOSITORY in 1 BLISTER PACK", "package_ndc": "76420-389-30", "marketing_start_date": "20250607"}], "brand_name": "Promethazine Hydrochloride", "product_id": "76420-389_36f60cbe-813d-cfa8-e063-6294a90a0b0a", "dosage_form": "SUPPOSITORY", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "76420-389", "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": "ANDA040500", "marketing_category": "ANDA", "marketing_start_date": "20060517", "listing_expiration_date": "20261231"}