NDC 52959-761

Clonazepam

Clonazepam

Clonazepam is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by H.j. Harkins Company, Inc.. The primary component is Clonazepam.

Product ID52959-761_8a441358-7fed-46d1-9401-ba50193cc639
NDC52959-761
Product TypeHuman Prescription Drug
Proprietary NameClonazepam
Generic NameClonazepam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-02-13
Marketing CategoryANDA / ANDA
Application NumberANDA074869
Labeler NameH.J. Harkins Company, Inc.
Substance NameCLONAZEPAM
Active Ingredient Strength2 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 52959-761-10

10 TABLET in 1 BOTTLE (52959-761-10)
Marketing Start Date2009-02-13
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 52959-761-00 [52959076100]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074869
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-02-13
Inactivation Date2019-11-13

NDC 52959-761-60 [52959076160]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074869
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-02-13
Inactivation Date2019-11-13

NDC 52959-761-30 [52959076130]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074869
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-02-13
Inactivation Date2019-11-13

NDC 52959-761-90 [52959076190]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074869
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-02-13
Inactivation Date2019-11-13

NDC 52959-761-10 [52959076110]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074869
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-02-13
Inactivation Date2019-11-13

Drug Details

Active Ingredients

IngredientStrength
CLONAZEPAM2 mg/1

OpenFDA Data

SPL SET ID:ec0e596c-baca-417d-8aa4-a1878100064d
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197527
  • 197528
  • 197529

    • Pharmacological Class

    • Benzodiazepine [EPC]
    • Benzodiazepines [CS]

    NDC Crossover Matching brand name "Clonazepam" or generic name "Clonazepam"

    NDCBrand NameGeneric Name
    0093-0832ClonazepamClonazepam
    0093-0833ClonazepamClonazepam
    0093-0834ClonazepamClonazepam
    0093-3212ClonazepamClonazepam
    0093-3213ClonazepamClonazepam
    0093-9290ClonazepamClonazepam
    0093-9291ClonazepamClonazepam
    68071-4021ClonazepamClonazepam
    68071-4135ClonazepamClonazepam
    68788-7181ClonazepamClonazepam
    68788-6989ClonazepamClonazepam
    68788-7394ClonazepamClonazepam
    68788-9379ClonazepamClonazepam
    68788-9941ClonazepamClonazepam
    68788-9378ClonazepamClonazepam
    68788-9495ClonazepamClonazepam
    68788-9940ClonazepamClonazepam
    0555-0098ClonazepamClonazepam
    0555-0096ClonazepamClonazepam
    0555-0094ClonazepamClonazepam
    0555-0095ClonazepamClonazepam
    0555-0097ClonazepamClonazepam
    70518-0154ClonazepamClonazepam
    70518-0259ClonazepamClonazepam
    70518-0644ClonazepamClonazepam
    70518-1353ClonazepamClonazepam
    70518-1199ClonazepamClonazepam
    70518-1069ClonazepamClonazepam
    70518-1559ClonazepamClonazepam
    70518-1521ClonazepamClonazepam
    70518-1297ClonazepamClonazepam
    70518-1945ClonazepamClonazepam
    70518-1801ClonazepamClonazepam
    0603-2948ClonazepamClonazepam
    71335-0001ClonazepamClonazepam
    71335-0022ClonazepamClonazepam
    71335-0113ClonazepamClonazepam
    71335-0333ClonazepamClonazepam
    71610-084ClonazepamClonazepam
    71610-023ClonazepamClonazepam
    71610-061ClonazepamClonazepam
    71610-040ClonazepamClonazepam
    71610-075ClonazepamClonazepam
    71610-039ClonazepamClonazepam
    71610-085ClonazepamClonazepam
    0615-7796ClonazepamClonazepam
    0615-8002ClonazepamClonazepam
    0615-8048ClonazepamClonazepam
    0615-8001ClonazepamClonazepam
    0615-8235ClonazepamClonazepam
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