NDC 62756-224

TIAGABINE HYDROCHLORIDE

Tiagabine Hydrochloride

TIAGABINE HYDROCHLORIDE is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is Tiagabine Hydrochloride.

Product ID62756-224_57975e74-e45b-4fd9-9718-bfc9690acae5
NDC62756-224
Product TypeHuman Prescription Drug
Proprietary NameTIAGABINE HYDROCHLORIDE
Generic NameTiagabine Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2011-11-04
Marketing CategoryANDA / ANDA
Application NumberANDA077555
Labeler NameSun Pharmaceutical Industries, Inc.
Substance NameTIAGABINE HYDROCHLORIDE
Active Ingredient Strength4 mg/1
Pharm ClassesAnti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 62756-224-08

100 TABLET, FILM COATED in 1 BOTTLE (62756-224-08)
Marketing Start Date2011-11-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62756-224-18 [62756022418]

TIAGABINE HYDROCHLORIDE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077555
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-11-04

NDC 62756-224-83 [62756022483]

TIAGABINE HYDROCHLORIDE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077555
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-11-04

NDC 62756-224-08 [62756022408]

TIAGABINE HYDROCHLORIDE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077555
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-11-04

NDC 62756-224-88 [62756022488]

TIAGABINE HYDROCHLORIDE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077555
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-11-04

Drug Details

Active Ingredients

IngredientStrength
TIAGABINE HYDROCHLORIDE4 mg/1

OpenFDA Data

SPL SET ID:7eeb2d81-c5d7-46a0-aa5c-149b55df71bd
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1299911
  • 1299917
    • UPC Code
  • 0362756200838
  • 0362756224834

    • Pharmacological Class

    • Anti-epileptic Agent [EPC]
    • Decreased Central Nervous System Disorganized Electrical Activity [PE]
    • Anti-epileptic Agent [EPC]
    • Decreased Central Nervous System Disorganized Electrical Activity [PE]

    Medicade Reported Pricing

    62756022483 TIAGABINE HCL 4 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "TIAGABINE HYDROCHLORIDE" or generic name "Tiagabine Hydrochloride"

    NDCBrand NameGeneric Name
    0093-5030Tiagabine HydrochlorideTiagabine Hydrochloride
    0093-5031Tiagabine HydrochlorideTiagabine Hydrochloride
    0093-8072Tiagabine HydrochlorideTiagabine Hydrochloride
    0093-8076Tiagabine HydrochlorideTiagabine Hydrochloride
    16714-151Tiagabine HydrochlorideTiagabine Hydrochloride
    16714-152Tiagabine HydrochlorideTiagabine Hydrochloride
    16714-153Tiagabine HydrochlorideTiagabine Hydrochloride
    16714-154Tiagabine HydrochlorideTiagabine Hydrochloride
    52536-350tiagabine hydrochloridetiagabine hydrochloride
    52536-355tiagabine hydrochloridetiagabine hydrochloride
    52536-360tiagabine hydrochloridetiagabine hydrochloride
    52536-365tiagabine hydrochloridetiagabine hydrochloride
    62756-200TIAGABINE HYDROCHLORIDETIAGABINE HYDROCHLORIDE
    62756-224TIAGABINE HYDROCHLORIDETIAGABINE HYDROCHLORIDE
    69238-1104Tiagabine HydrochlorideTiagabine Hydrochloride
    69238-1107Tiagabine HydrochlorideTiagabine Hydrochloride
    69238-1105Tiagabine HydrochlorideTiagabine Hydrochloride
    69238-1106Tiagabine HydrochlorideTiagabine Hydrochloride
    63459-402GABITRILTiagabine Hydrochloride
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