NDC 68788-6942

Diazepam

Diazepam

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

Product ID68788-6942_ea788ea5-7082-4d1c-ab94-0224b6cabd88
NDC68788-6942
Product TypeHuman Prescription Drug
Proprietary NameDiazepam
Generic NameDiazepam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-04-05
Marketing CategoryANDA / ANDA
Application NumberANDA071136
Labeler NamePreferred Pharmaceuticals Inc.
Substance NameDIAZEPAM
Active Ingredient Strength10 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 68788-6942-4

10 TABLET in 1 BOTTLE, PLASTIC (68788-6942-4)
Marketing Start Date2017-04-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-6942-6 [68788694206]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-04-05
Inactivation Date2020-01-31

NDC 68788-6942-5 [68788694205]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-04-05
Inactivation Date2020-01-31

NDC 68788-6942-9 [68788694209]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-04-05
Inactivation Date2020-01-31

NDC 68788-6942-4 [68788694204]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-04-05
Inactivation Date2020-01-31

NDC 68788-6942-1 [68788694201]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-04-05
Inactivation Date2020-01-31

NDC 68788-6942-0 [68788694200]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-04-05
Inactivation Date2020-01-31

NDC 68788-6942-2 [68788694202]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-04-05
Inactivation Date2020-01-31

NDC 68788-6942-3 [68788694203]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-04-05
Inactivation Date2020-01-31

NDC 68788-6942-8 [68788694208]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-04-05
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
DIAZEPAM10 mg/1

OpenFDA Data

SPL SET ID:771ab1ea-cd81-4c66-b674-da23720f350a
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197589
  • 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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