Package 70518-3549-0

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3549-0
Digits Only 7051835490
Product NDC 70518-3549
Description

30 TABLET, SUGAR COATED in 1 BLISTER PACK (70518-3549-0)

Marketing

Marketing Status
Marketed Since 2022-10-03
Brand chlorpromazine hydrochloride
Generic chlorpromazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a924606-27bd-8424-e063-6394a90a0fb7", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991336"], "spl_set_id": ["c2a38be8-43e6-4a56-9556-fe3dad412b82"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, SUGAR COATED in 1 BLISTER PACK (70518-3549-0)", "package_ndc": "70518-3549-0", "marketing_start_date": "20221003"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-3549-1)  / 1 TABLET, SUGAR COATED in 1 POUCH (70518-3549-2)", "package_ndc": "70518-3549-1", "marketing_start_date": "20240419"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "70518-3549_4a924606-27bd-8424-e063-6394a90a0fb7", "dosage_form": "TABLET, SUGAR COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-3549", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA214827", "marketing_category": "ANDA", "marketing_start_date": "20221003", "listing_expiration_date": "20271231"}