Package 70518-3670-0

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3670-0
Digits Only 7051836700
Product NDC 70518-3670
Product ID 70518-3670_3b024cbf-81d0-0dc7-e063-6294a90a81ee
Description

100 POUCH in 1 BOX (70518-3670-0) / 1 TABLET, COATED in 1 POUCH (70518-3670-1)

Marketing

Marketing Status
Marketed Since 2023-03-03
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": "3b024cbf-81d0-0dc7-e063-6294a90a81ee", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991044"], "spl_set_id": ["023e19a1-0d2d-49e6-a9af-fbbeb7a33c5f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-3670-0)  / 1 TABLET, COATED in 1 POUCH (70518-3670-1)", "package_ndc": "70518-3670-0", "marketing_start_date": "20230303"}], "brand_name": "Chlorpromazine Hydrochloride", "product_id": "70518-3670_3b024cbf-81d0-0dc7-e063-6294a90a81ee", "dosage_form": "TABLET, COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-3670", "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": "ANDA212996", "marketing_category": "ANDA", "marketing_start_date": "20230303", "listing_expiration_date": "20261231"}