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NDC 70518-3095-00 Fluphenazine Hydrochloride 5 mg/1 Details
Fluphenazine Hydrochloride 5 mg/1
Fluphenazine Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK 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: 70518-3095-00Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Fluphenazine
Product Information
NDC | 70518-3095 |
---|---|
Product ID | 70518-3095_f70afd80-23f5-a3b4-e053-6394a90a187b |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Fluphenazine Hydrochloride |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Fluphenazine Hydrochloride |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET |
Route | ORAL |
Active Ingredient Strength | 5 |
Active Ingredient Units | mg/1 |
Substance Name | FLUPHENAZINE HYDROCHLORIDE |
Labeler Name | REMEDYREPACK INC. |
Pharmaceutical Class | Phenothiazine [EPC], Phenothiazines [CS] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA214674 |
Listing Certified Through | 2024-12-31 |
Package
NDC 70518-3095-00 (70518309500)
NDC Package Code | 70518-3095-0 |
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Billing NDC | 70518309500 |
Package | 30 TABLET in 1 BLISTER PACK (70518-3095-0) |
Marketing Start Date | 2021-05-17 |
NDC Exclude Flag | N |
Pricing Information | N/A |