Package 70518-3510-0

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3510-0
Digits Only 7051835100
Product NDC 70518-3510
Product ID 70518-3510_4c0e03ae-d19e-a44f-e063-6294a90a58bf
Description

30 TABLET, SUGAR COATED in 1 BLISTER PACK (70518-3510-0)

Marketing

Marketing Status
Marketed Since 2022-09-06
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": ["ORAL"], "spl_id": "4c0e03ae-d19e-a44f-e063-6294a90a58bf", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991194"], "spl_set_id": ["2122d619-3f5b-48f6-8f0b-7693199abbdb"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, SUGAR COATED in 1 BLISTER PACK (70518-3510-0)", "package_ndc": "70518-3510-0", "marketing_start_date": "20220906"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "70518-3510_4c0e03ae-d19e-a44f-e063-6294a90a58bf", "dosage_form": "TABLET, SUGAR COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-3510", "generic_name": "Chlorpromazine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine Hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA214827", "marketing_category": "ANDA", "marketing_start_date": "20220906", "listing_expiration_date": "20271231"}