Package 51079-572-20

Brand: trifluoperazine hydrochloride

Generic: trifluoperazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51079-572-20
Digits Only 5107957220
Product NDC 51079-572
Product ID 51079-572_3a877366-459b-cfac-e063-6294a90a6453
Description

100 BLISTER PACK in 1 CARTON (51079-572-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-572-01)

Marketing

Marketing Status
Marketed Since 1998-03-04
Brand trifluoperazine hydrochloride
Generic trifluoperazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Trifluoperazine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3a877366-459b-cfac-e063-6294a90a6453", "openfda": {"unii": ["6P1Y2SNF5V"], "rxcui": ["198322", "198323", "198324", "198325"], "spl_set_id": ["f742a579-411a-4140-91c4-edc735d638fa"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-572-20)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-572-01)", "package_ndc": "51079-572-20", "marketing_start_date": "19980304"}], "brand_name": "Trifluoperazine Hydrochloride", "product_id": "51079-572_3a877366-459b-cfac-e063-6294a90a6453", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "51079-572", "generic_name": "trifluoperazine hydrochloride", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trifluoperazine Hydrochloride", "active_ingredients": [{"name": "TRIFLUOPERAZINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA040209", "marketing_category": "ANDA", "marketing_start_date": "19980304", "listing_expiration_date": "20261231"}