Package 84549-525-03

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84549-525-03
Digits Only 8454952503
Product NDC 84549-525
Description

1 mL in 1 AMPULE (84549-525-03)

Marketing

Marketing Status
Marketed Since 2025-12-11
Brand promethazine hydrochloride
Generic promethazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "45b09a50-dab1-e83d-e063-6394a90aa813", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992460"], "spl_set_id": ["45b09a50-dab2-e83d-e063-6394a90aa813"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 AMPULE (84549-525-03)", "package_ndc": "84549-525-03", "marketing_start_date": "20251211"}], "brand_name": "PROMETHAZINE HYDROCHLORIDE", "product_id": "84549-525_45b09a50-dab1-e83d-e063-6394a90aa813", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "84549-525", "generic_name": "PROMETHAZINE HYDROCHLORIDE", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROMETHAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "PROMETHAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA040737", "marketing_category": "ANDA", "marketing_start_date": "20150130", "listing_expiration_date": "20261231"}