NDC 67046-920

Clonazepam

Clonazepam

Clonazepam is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Contract Pharmacy Services-pa. The primary component is Clonazepam.

Product ID67046-920_5a43c270-d2fb-a326-e053-2991aa0a5d95
NDC67046-920
Product TypeHuman Prescription Drug
Proprietary NameClonazepam
Generic NameClonazepam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-09-28
Marketing CategoryANDA / ANDA
Application NumberANDA074569
Labeler NameContract Pharmacy Services-PA
Substance NameCLONAZEPAM
Active Ingredient Strength2 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 67046-920-07

7 TABLET in 1 BLISTER PACK (67046-920-07)
Marketing Start Date2017-09-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67046-920-20 [67046092020]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074569
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

NDC 67046-920-14 [67046092014]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074569
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

NDC 67046-920-15 [67046092015]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074569
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

NDC 67046-920-28 [67046092028]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074569
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

NDC 67046-920-30 [67046092030]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074569
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

NDC 67046-920-21 [67046092021]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074569
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

NDC 67046-920-60 [67046092060]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074569
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

NDC 67046-920-07 [67046092007]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA074569
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

Drug Details

Active Ingredients

IngredientStrength
CLONAZEPAM2 mg/1

OpenFDA Data

SPL SET ID:5a43c270-d2fa-a326-e053-2991aa0a5d95
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197527
  • 197529
    • UPC Code
  • 0300930834059
  • 0300930832055

    • Pharmacological Class

    • Benzodiazepine [EPC]
    • Benzodiazepines [CS]
    • 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.