NDC 67544-020

Diazepam

Diazepam

Diazepam is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Aphena Pharma Solutions - Tennessee, Llc. The primary component is Diazepam.

Product ID67544-020_9286513a-0020-4199-ab54-c5da4831bb64
NDC67544-020
Product TypeHuman Prescription Drug
Proprietary NameDiazepam
Generic NameDiazepam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1987-02-03
Marketing CategoryANDA / ANDA
Application NumberANDA071136
Labeler NameAphena Pharma Solutions - Tennessee, LLC
Substance NameDIAZEPAM
Active Ingredient Strength10 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 67544-020-15

15 TABLET in 1 BOTTLE, PLASTIC (67544-020-15)
Marketing Start Date2009-02-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67544-020-90 [67544002090]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-02-05

NDC 67544-020-15 [67544002015]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-02-05

NDC 67544-020-45 [67544002045]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-12-12

NDC 67544-020-80 [67544002080]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-12-12

NDC 67544-020-53 [67544002053]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-12-12

NDC 67544-020-70 [67544002070]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-12-12

NDC 67544-020-75 [67544002075]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-05-15

NDC 67544-020-60 [67544002060]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-12-12

NDC 67544-020-30 [67544002030]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071136
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-12-12

Drug Details

Active Ingredients

IngredientStrength
DIAZEPAM10 mg/1

OpenFDA Data

SPL SET ID:283f5373-afce-47e1-9fb4-f5b80d6014c7
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197589
  • Pharmacological Class

    • Benzodiazepine [EPC]
    • Benzodiazepines [CS]
    • 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

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.