NDC 21695-134

Trazodone Hydrochloride

Trazodone

Trazodone Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Rebel Distributors Corp.. The primary component is Trazodone Hydrochloride.

Product ID21695-134_370453cb-7636-43f2-93f0-e8714884fab4
NDC21695-134
Product TypeHuman Prescription Drug
Proprietary NameTrazodone Hydrochloride
Generic NameTrazodone
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1987-12-11
Marketing CategoryANDA / ANDA
Application NumberANDA071524
Labeler NameRebel Distributors Corp.
Substance NameTRAZODONE HYDROCHLORIDE
Active Ingredient Strength100 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 21695-134-60

60 TABLET in 1 BOTTLE (21695-134-60)
Marketing Start Date1987-12-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 21695-134-90 [21695013490]

Trazodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA071524
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1987-12-11
Inactivation Date2019-09-24

NDC 21695-134-60 [21695013460]

Trazodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA071524
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1987-12-11
Inactivation Date2019-09-24

NDC 21695-134-30 [21695013430]

Trazodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA071524
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1987-12-11
Inactivation Date2019-09-24

Drug Details

Active Ingredients

IngredientStrength
TRAZODONE HYDROCHLORIDE100 mg/1

OpenFDA Data

SPL SET ID:6f43cdc2-4f8e-4a5f-976a-d3aaac65593d
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 856364
  • 856373
  • 856377
  • Pharmacological Class

    • Serotonin Reuptake Inhibitor [EPC]