NDC 52959-306

DIAZEPAM

Diazepam

DIAZEPAM is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by H.j. Harkins Company, Inc.. The primary component is Diazepam.

Product ID52959-306_75c7d502-0179-5ba1-e053-2a91aa0a7d67
NDC52959-306
Product TypeHuman Prescription Drug
Proprietary NameDIAZEPAM
Generic NameDiazepam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-01-25
Marketing CategoryANDA / ANDA
Application NumberANDA071136
Labeler NameH.J. Harkins Company, 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 52959-306-06

6 TABLET in 1 BOTTLE (52959-306-06)
Marketing Start Date2016-01-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 52959-306-15 [52959030615]

DIAZEPAM TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-01-25
Inactivation Date2020-01-31

NDC 52959-306-30 [52959030630]

DIAZEPAM TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-01-25
Inactivation Date2020-01-31

NDC 52959-306-60 [52959030660]

DIAZEPAM TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-01-25
Inactivation Date2020-01-31

NDC 52959-306-00 [52959030600]

DIAZEPAM TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-01-25
Inactivation Date2020-01-31

NDC 52959-306-45 [52959030645]

DIAZEPAM TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-01-25
Inactivation Date2020-01-31

NDC 52959-306-06 [52959030606]

DIAZEPAM TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-01-25
Inactivation Date2020-01-31

NDC 52959-306-20 [52959030620]

DIAZEPAM TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-01-25
Inactivation Date2020-01-31

NDC 52959-306-90 [52959030690]

DIAZEPAM TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-01-25
Inactivation Date2020-01-31

NDC 52959-306-02 [52959030602]

DIAZEPAM TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-01-25
Inactivation Date2020-01-31

NDC 52959-306-01 [52959030601]

DIAZEPAM TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-01-25
Inactivation Date2020-01-31

NDC 52959-306-10 [52959030610]

DIAZEPAM TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-01-25
Inactivation Date2020-01-31

NDC 52959-306-05 [52959030605]

DIAZEPAM TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-01-25
Inactivation Date2020-01-31

NDC 52959-306-28 [52959030628]

DIAZEPAM TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-01-25
Inactivation Date2020-01-31

NDC 52959-306-14 [52959030614]

DIAZEPAM TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-01-25
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
DIAZEPAM10 mg/1

OpenFDA Data

SPL SET ID:75c7d502-0178-5ba1-e053-2a91aa0a7d67
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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