Package 73043-049-25

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 73043-049-25
Digits Only 7304304925
Product NDC 73043-049
Product ID 73043-049_4635d706-5e3d-4817-bf04-802a20f72a70
Description

25 AMPULE in 1 CARTON (73043-049-25) / 2 mL in 1 AMPULE (73043-049-01)

Marketing

Marketing Status
Marketed Since 2024-11-01
Brand chlorpromazine hydrochloride
Generic chlorpromazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Chlorpromazine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "4635d706-5e3d-4817-bf04-802a20f72a70", "openfda": {"upc": ["0373043048255", "0373043049252"], "unii": ["9WP59609J6"], "rxcui": ["1730076", "1730078"], "spl_set_id": ["b73b9044-7132-41b7-83d4-2d135ea831f1"], "manufacturer_name": ["Devatis, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 AMPULE in 1 CARTON (73043-049-25)  / 2 mL in 1 AMPULE (73043-049-01)", "package_ndc": "73043-049-25", "marketing_start_date": "20241101"}], "brand_name": "Chlorpromazine hydrochloride", "product_id": "73043-049_4635d706-5e3d-4817-bf04-802a20f72a70", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "73043-049", "generic_name": "Chlorpromazine hydrochloride", "labeler_name": "Devatis, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA218229", "marketing_category": "ANDA", "marketing_start_date": "20241101", "listing_expiration_date": "20261231"}