NDC 70518-1353

Clonazepam

Clonazepam

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

Product ID70518-1353_72f3a0ab-7dbb-cae9-e053-2a91aa0a70e4
NDC70518-1353
Product TypeHuman Prescription Drug
Proprietary NameClonazepam
Generic NameClonazepam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2018-08-08
Marketing CategoryANDA / ANDA
Application NumberANDA077856
Labeler NameREMEDYREPACK 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 70518-1353-0

30 TABLET in 1 BLISTER PACK (70518-1353-0)
Marketing Start Date2018-08-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70518-1353-1 [70518135301]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA077856
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-16

NDC 70518-1353-2 [70518135302]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA077856
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-17

NDC 70518-1353-0 [70518135300]

Clonazepam TABLET
Marketing CategoryANDA
Application NumberANDA077856
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-08-08

Drug Details

Active Ingredients

IngredientStrength
CLONAZEPAM1 mg/1

OpenFDA Data

SPL SET ID:bca43c08-2141-4c02-95d4-01756557b6c2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 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.