NDC 0555-0097

Clonazepam

Clonazepam

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

Product ID0555-0097_2a5bb522-a84e-47ea-bad8-3af66c3a763a
NDC0555-0097
Product TypeHuman Prescription Drug
Proprietary NameClonazepam
Generic NameClonazepam
Dosage FormTablet, Orally Disintegrating
Route of AdministrationORAL
Marketing Start Date2005-08-11
Marketing CategoryANDA / ANDA
Application NumberANDA077194
Labeler NameTeva Pharmaceuticals USA, Inc.
Substance NameCLONAZEPAM
Active Ingredient Strength1 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0555-0097-96

10 BLISTER PACK in 1 CARTON (0555-0097-96) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Marketing Start Date2005-08-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0555-0097-96 [00555009796]

Clonazepam TABLET, ORALLY DISINTEGRATING
Marketing CategoryANDA
Application NumberANDA077194
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-08-11

Drug Details

Active Ingredients

IngredientStrength
CLONAZEPAM1 mg/1

OpenFDA Data

SPL SET ID:7fe78a8d-1e6a-431e-958e-f1f1b420efa2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 349196
  • 349197
  • 349194
  • 349195
  • 349198
  • 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.