NDC 63629-2956

Triazolam

Triazolam

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

Product ID63629-2956_12c0c495-a032-382e-9b04-37018090cad0
NDC63629-2956
Product TypeHuman Prescription Drug
Proprietary NameTriazolam
Generic NameTriazolam
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2018-10-29
Marketing CategoryANDA / ANDA
Application NumberANDA074224
Labeler NameBryant Ranch Prepack
Substance NameTRIAZOLAM
Active Ingredient Strength0 mg/1
Pharm ClassesBenzodiazepine [EPC],Benzodiazepines [CS]
DEA ScheduleCIV
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 63629-2956-0

3 TABLET in 1 BOTTLE (63629-2956-0)
Marketing Start Date2021-12-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-2956-9 [63629295609]

Triazolam TABLET
Marketing CategoryANDA
Application NumberANDA074224
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-10-29
Marketing End Date2018-10-31

NDC 63629-2956-7 [63629295607]

Triazolam TABLET
Marketing CategoryANDA
Application NumberANDA074224
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-10-29
Marketing End Date2018-10-31

NDC 63629-2956-2 [63629295602]

Triazolam TABLET
Marketing CategoryANDA
Application NumberANDA074224
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-10-29
Marketing End Date2018-10-31

NDC 63629-2956-0 [63629295600]

Triazolam TABLET
Marketing CategoryANDA
Application NumberANDA074224
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-10-29
Marketing End Date2018-10-31

NDC 63629-2956-8 [63629295608]

Triazolam TABLET
Marketing CategoryANDA
Application NumberANDA074224
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-10-29
Marketing End Date2018-10-31

NDC 63629-2956-5 [63629295605]

Triazolam TABLET
Marketing CategoryANDA
Application NumberANDA074224
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-10-29
Marketing End Date2018-10-31

NDC 63629-2956-3 [63629295603]

Triazolam TABLET
Marketing CategoryANDA
Application NumberANDA074224
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-10-29
Marketing End Date2018-10-31

NDC 63629-2956-4 [63629295604]

Triazolam TABLET
Marketing CategoryANDA
Application NumberANDA074224
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-10-29
Marketing End Date2018-10-31

NDC 63629-2956-1 [63629295601]

Triazolam TABLET
Marketing CategoryANDA
Application NumberANDA074224
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-10-29
Marketing End Date2018-10-31

NDC 63629-2956-6 [63629295606]

Triazolam TABLET
Marketing CategoryANDA
Application NumberANDA074224
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-10-29
Marketing End Date2018-10-31

Drug Details

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

NDCBrand NameGeneric Name
0054-4858TriazolamTriazolam
0054-4859TriazolamTriazolam
21695-284TriazolamTriazolam
21695-303TriazolamTriazolam
43063-996TriazolamTriazolam
43353-451Triazolamtriazolam
50090-0522Triazolamtriazolam
50090-4733TriazolamTriazolam
50436-3718Triazolamtriazolam
50742-645TriazolamTriazolam
50742-646TriazolamTriazolam
55289-787Triazolamtriazolam
59762-3717Triazolamtriazolam
59762-3718Triazolamtriazolam
67544-725TriazolamTriazolam
63629-2956TriazolamTriazolam
0009-0017Halciontriazolam

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