Package 39822-5525-3

Brand: promethazine hydrochloride

Generic: promethazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 39822-5525-3
Digits Only 3982255253
Product NDC 39822-5525
Description

25 AMPULE in 1 CARTON (39822-5525-3) / 1 mL in 1 AMPULE (39822-5525-2)

Marketing

Marketing Status
Marketed Since 2015-01-30
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": "0e3526e1-38be-1d89-e063-6294a90a775d", "openfda": {"unii": ["R61ZEH7I1I"], "rxcui": ["992460"], "spl_set_id": ["1d02d52b-84bb-4e81-b352-125029eb39f6"], "manufacturer_name": ["XGen Pharmaceuticals DJB, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 AMPULE in 1 CARTON (39822-5525-3)  / 1 mL in 1 AMPULE (39822-5525-2)", "package_ndc": "39822-5525-3", "marketing_start_date": "20150130"}], "brand_name": "PROMETHAZINE HYDROCHLORIDE", "product_id": "39822-5525_0e3526e1-38be-1d89-e063-6294a90a775d", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "39822-5525", "generic_name": "PROMETHAZINE HYDROCHLORIDE", "labeler_name": "XGen Pharmaceuticals DJB, Inc.", "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"}