Package 0904-7304-61

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7304-61
Digits Only 0904730461
Product NDC 0904-7304
Product ID 0904-7304_483c6903-10ec-4665-9dba-8073728937cf
Description

100 BLISTER PACK in 1 CARTON (0904-7304-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2023-04-17
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": "483c6903-10ec-4665-9dba-8073728937cf", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992447"], "spl_set_id": ["4cee8622-7d59-4794-8e32-54f7aac1d923"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7304-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7304-61", "marketing_start_date": "20230417"}], "brand_name": "Promethazine Hydrochloride", "product_id": "0904-7304_483c6903-10ec-4665-9dba-8073728937cf", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0904-7304", "generic_name": "Promethazine Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Promethazine Hydrochloride", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA091179", "marketing_category": "ANDA", "marketing_start_date": "20230417", "listing_expiration_date": "20261231"}