Package 0378-2401-01

Brand: trifluoperazine hydrochloride

Generic: trifluoperazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0378-2401-01
Digits Only 0378240101
Product NDC 0378-2401
Product ID 0378-2401_7586125c-d9c7-4c56-8ca8-8add657a91db
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-2401-01)

Marketing

Marketing Status
Marketed Since 1997-08-29
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": "7586125c-d9c7-4c56-8ca8-8add657a91db", "openfda": {"upc": ["0303782402018", "0303782405019"], "unii": ["6P1Y2SNF5V"], "rxcui": ["198322", "198323", "198324", "198325"], "spl_set_id": ["c2575a86-19e5-44df-8603-ff066bb9c9c5"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-2401-01)", "package_ndc": "0378-2401-01", "marketing_start_date": "19970829"}], "brand_name": "Trifluoperazine Hydrochloride", "product_id": "0378-2401_7586125c-d9c7-4c56-8ca8-8add657a91db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0378-2401", "generic_name": "trifluoperazine hydrochloride", "labeler_name": "Mylan Pharmaceuticals 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": "19970829", "listing_expiration_date": "20261231"}