Package 16714-051-01

Brand: chlorpromazine hydrochloride

Generic: chlorpromazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16714-051-01
Digits Only 1671405101
Product NDC 16714-051
Product ID 16714-051_13fe8f97-37e8-4d10-87fe-e1d17f4f23d8
Description

100 TABLET, FILM COATED in 1 BOTTLE (16714-051-01)

Marketing

Marketing Status
Marketed Since 2020-05-11
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": "13fe8f97-37e8-4d10-87fe-e1d17f4f23d8", "openfda": {"unii": ["9WP59609J6"], "rxcui": ["991039", "991044", "991188", "991194", "991336"], "spl_set_id": ["2bd42d3a-bf89-4d74-a252-9b914106a570"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16714-051-01)", "package_ndc": "16714-051-01", "marketing_start_date": "20200511"}], "brand_name": "Chlorpromazine hydrochloride", "product_id": "16714-051_13fe8f97-37e8-4d10-87fe-e1d17f4f23d8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "16714-051", "generic_name": "Chlorpromazine hydrochloride", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorpromazine hydrochloride", "active_ingredients": [{"name": "CHLORPROMAZINE HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA213368", "marketing_category": "ANDA", "marketing_start_date": "20200511", "listing_expiration_date": "20261231"}