Package 70518-4294-0

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4294-0
Digits Only 7051842940
Product NDC 70518-4294
Product ID 70518-4294_401ccac6-a5d6-bf76-e063-6294a90a87f0
Description

100 POUCH in 1 BOX (70518-4294-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4294-1)

Marketing

Marketing Status
Marketed Since 2025-02-26
Brand chlorpromazine hydrochloride
Generic chlorpromazine hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "401ccac6-a5d6-bf76-e063-6294a90a87f0", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991044"], "spl_set_id": ["9709ffde-7034-42be-97be-f5f39eeacf72"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-4294-0)  / 1 TABLET, FILM COATED in 1 POUCH (70518-4294-1)", "package_ndc": "70518-4294-0", "marketing_start_date": "20250226"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "70518-4294_401ccac6-a5d6-bf76-e063-6294a90a87f0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-4294", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA084114", "marketing_category": "ANDA", "marketing_start_date": "20250226", "listing_expiration_date": "20261231"}