NDC 71335-0616

Diazepam

Diazepam

Diazepam is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Diazepam.

Product ID71335-0616_1e07badc-1669-4345-94ca-475f664c0e69
NDC71335-0616
Product TypeHuman Prescription Drug
Proprietary NameDiazepam
Generic NameDiazepam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-08-03
Marketing CategoryANDA / ANDA
Application NumberANDA071134
Labeler NameBryant Ranch Prepack
Substance NameDIAZEPAM
Active Ingredient Strength2 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 71335-0616-1

30 TABLET in 1 BOTTLE (71335-0616-1)
Marketing Start Date2017-12-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0616-7 [71335061607]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071134
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-12-06

NDC 71335-0616-2 [71335061602]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071134
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-12-06

NDC 71335-0616-1 [71335061601]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071134
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-12-06

NDC 71335-0616-8 [71335061608]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071134
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-12-06

NDC 71335-0616-5 [71335061605]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071134
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-12-06

NDC 71335-0616-6 [71335061606]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071134
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-12-06

NDC 71335-0616-4 [71335061604]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071134
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-12-06

NDC 71335-0616-3 [71335061603]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071134
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-12-06

Drug Details

Active Ingredients

IngredientStrength
DIAZEPAM2 mg/1

OpenFDA Data

SPL SET ID:3ccd7dc7-eff4-42bf-b538-610996192881
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197589
  • 197591
  • 197590
  • Pharmacological Class

    • Benzodiazepine [EPC]
    • Benzodiazepines [CS]

    NDC Crossover Matching brand name "Diazepam" or generic name "Diazepam"

    NDCBrand NameGeneric Name
    0054-3188DiazepamDiazepam
    0093-6137DiazepamDiazepam
    0093-6138DiazepamDiazepam
    0093-6139DiazepamDiazepam
    0121-0905DiazepamDiazepam
    0172-3925DiazepamDiazepam
    0172-3926DiazepamDiazepam
    0172-3927DiazepamDiazepam
    68071-4030DiazepamDiazepam
    68071-3330DiazepamDiazepam
    68071-3270DiazepamDiazepam
    68071-4181DiazepamDiazepam
    68071-4770DiazepamDiazepam
    68071-4829DiazepamDiazepam
    68094-750DiazepamDiazepam
    68682-652DiazepamDiazepam
    68682-650DiazepamDiazepam
    68682-655DiazepamDiazepam
    68788-6942DiazepamDiazepam
    68788-9207DiazepamDiazepam
    68788-6851DiazepamDiazepam
    68788-9937DiazepamDiazepam
    68788-9208DiazepamDiazepam
    68788-9936DiazepamDiazepam
    0527-1768DiazepamDiazepam
    0527-1767DiazepamDiazepam
    69339-136DiazepamDiazepam
    70518-0162DiazepamDiazepam
    70518-0014DiazepamDiazepam
    70518-1713DiazepamDiazepam
    70518-1270DiazepamDiazepam
    70518-1856DiazepamDiazepam
    0603-3215DiazepamDiazepam
    71335-0142DiazepamDiazepam
    71335-0444DiazepamDiazepam
    71335-0495DiazepamDiazepam
    71335-0616DiazepamDiazepam
    0615-7800DiazepamDiazepam
    0615-8049DiazepamDiazepam
    0904-5880DiazepamDiazepam
    10544-161DiazepamDiazepam
    11704-600DiazepamDiazepam
    12634-698DIAZEPAMDIAZEPAM
    12634-529DIAZEPAMDIAZEPAM
    17856-3188DiazepamDiazepam
    21695-265DiazepamDiazepam
    21695-264DiazepamDiazepam
    21695-889DiazepamDiazepam
    21695-263DiazepamDiazepam
    33261-034DiazepamDiazepam

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