NDC 0603-2948

Clonazepam

Clonazepam

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

Product ID0603-2948_afc11554-19f4-4e13-a4d5-0357524325eb
NDC0603-2948
Product TypeHuman Prescription Drug
Proprietary NameClonazepam
Generic NameClonazepam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2006-06-28
Marketing End Date2019-09-30
Marketing CategoryANDA / ANDA
Application NumberANDA077856
Labeler NameQualitest Pharmaceuticals
Substance NameCLONAZEPAM
Active Ingredient Strength1 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagN

Packaging

NDC 0603-2948-60

45 TABLET in 1 BOTTLE, PLASTIC (0603-2948-60)
Marketing Start Date2006-06-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0603-2948-26 [00603294826]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA077856
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-06-28
Marketing End Date2019-09-30

NDC 0603-2948-16 [00603294816]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA077856
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-06-28
Marketing End Date2019-09-30

NDC 0603-2948-28 [00603294828]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA077856
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-06-28
Marketing End Date2019-09-30

NDC 0603-2948-21 [00603294821]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA077856
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-06-28
Marketing End Date2019-09-30

NDC 0603-2948-13 [00603294813]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA077856
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-06-28
Marketing End Date2019-09-30

NDC 0603-2948-60 [00603294860]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA077856
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-06-28
Marketing End Date2019-09-30

NDC 0603-2948-20 [00603294820]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA077856
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-06-28
Marketing End Date2019-09-30

NDC 0603-2948-22 [00603294822]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA077856
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-06-28
Marketing End Date2019-09-30

NDC 0603-2948-02 [00603294802]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA077856
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-06-28
Marketing End Date2019-09-30

NDC 0603-2948-32 [00603294832]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA077856
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-06-28
Marketing End Date2019-09-30

NDC 0603-2948-10 [00603294810]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA077856
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-06-28
Marketing End Date2016-05-20

Drug Details

Active Ingredients

IngredientStrength
CLONAZEPAM.5 mg/1

OpenFDA Data

SPL SET ID:eb75c672-8c72-4967-b97b-4119d49a9cb1
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197527
  • 197528
  • 197529
    • UPC Code
  • 0306032949219
  • 0306032948212
  • 0306032950215

    • 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.