NDC 49999-018

Diazepam

Diazepam

Diazepam is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Lake Erie Medical Dba Qua. The primary component is Diazepam.

Product ID49999-018_7b51a199-f55a-4e0d-8bc9-2afe2887c95b
NDC49999-018
Product TypeHuman Prescription Drug
Proprietary NameDiazepam
Generic NameDiazepam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2011-11-29
Marketing CategoryANDA / ANDA
Application NumberANDA071321
Labeler NameLake Erie Medical DBA Qua
Substance NameDIAZEPAM
Active Ingredient Strength5 mg/1
Pharm ClassesBenzodiazepine
DEA ScheduleCIV
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 49999-018-10

10 TABLET in 1 BOTTLE (49999-018-10)
Marketing Start Date2011-11-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49999-018-05 [49999001805]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071321
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-11-29
Marketing End Date2014-06-01

NDC 49999-018-30 [49999001830]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071321
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-11-29

NDC 49999-018-02 [49999001802]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071321
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-11-29
Marketing End Date2014-06-01

NDC 49999-018-15 [49999001815]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071321
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-11-29
Marketing End Date2014-06-01

NDC 49999-018-60 [49999001860]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071321
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-11-29

NDC 49999-018-10 [49999001810]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071321
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-11-29

NDC 49999-018-90 [49999001890]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071321
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-11-29

NDC 49999-018-20 [49999001820]

Diazepam TABLET
Marketing CategoryANDA
Application NumberANDA071321
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-11-29

Drug Details

Active Ingredients

IngredientStrength
DIAZEPAM5 mg/1

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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