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NDC 70710-1489-05 Fluphenazine Hydrochloride 2.5 mg/1 Details

Fluphenazine Hydrochloride 2.5 mg/1

Fluphenazine Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals (USA) Inc.. The primary component is FLUPHENAZINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Fluphenazine is an antipsychotic medication used to treat schizophrenia and psychotic symptoms such as hallucinations, delusions, and hostility. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 70710-1489-05
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Fluphenazine

Product Information

NDC	70710-1489
Product ID	70710-1489_f3b6f558-bb8c-46ce-990f-7d07a807a4b5
Associated GPIs	59200025100310
GCN Sequence Number	003825
GCN Sequence Number Description	fluphenazine HCl TABLET 2.5 MG ORAL
HIC3	H2G
HIC3 Description	ANTIPSYCHOTICS,PHENOTHIAZINES
GCN	14604
HICL Sequence Number	001626
HICL Sequence Number Description	FLUPHENAZINE HCL
Brand/Generic	Generic
Proprietary Name	Fluphenazine Hydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	Fluphenazine Hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	2.5
Active Ingredient Units	mg/1
Substance Name	FLUPHENAZINE HYDROCHLORIDE
Labeler Name	Zydus Pharmaceuticals (USA) Inc.
Pharmaceutical Class	Phenothiazine [EPC], Phenothiazines [CS]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA214552
Listing Certified Through	2024-12-31

Package

NDC 70710-1489-05 (70710148905)

Pricing Information	N/A
NDC Package Code	70710-1489-5
Billing NDC	70710148905
Package	500 TABLET, FILM COATED in 1 BOTTLE (70710-1489-5)
Marketing Start Date	2021-05-28
NDC Exclude Flag	N