NDC 68788-9940

Clonazepam

Clonazepam

Clonazepam is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is Clonazepam.

Product ID68788-9940_6c4bb73e-a61d-4413-86e9-31cdd5bcdef7
NDC68788-9940
Product TypeHuman Prescription Drug
Proprietary NameClonazepam
Generic NameClonazepam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2012-01-17
Marketing CategoryANDA / ANDA
Application NumberANDA074869
Labeler NamePreferred Pharmaceuticals, Inc.
Substance NameCLONAZEPAM
Active Ingredient Strength1 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 68788-9940-9

90 TABLET in 1 BOTTLE (68788-9940-9)
Marketing Start Date2012-01-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-9940-2 [68788994002]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074869
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-01-17
Marketing End Date2019-08-07

NDC 68788-9940-6 [68788994006]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074869
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-01-17
Marketing End Date2019-08-07

NDC 68788-9940-3 [68788994003]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074869
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-01-17
Marketing End Date2019-08-07

NDC 68788-9940-9 [68788994009]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074869
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-01-17
Marketing End Date2019-08-07

NDC 68788-9940-8 [68788994008]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074869
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-01-17
Marketing End Date2019-08-07

Drug Details

Active Ingredients

IngredientStrength
CLONAZEPAM1 mg/1

OpenFDA Data

SPL SET ID:4d586471-8b20-4899-94ad-31e0a519e99e
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197527
  • 197528
  • 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

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.