NDC 51655-634

TRAZODONE

Trazodone

TRAZODONE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Northwind Pharmaceuticals, Llc. The primary component is Trazodone Hydrochloride.

• Product ID: 51655-634_ae73e6db-4fa3-459c-8b14-11d4404a183c
• NDC: 51655-634
• Product Type: Human Prescription Drug
• Proprietary Name: TRAZODONE
• Generic Name: Trazodone
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2014-12-01
• Marketing Category: ANDA / ANDA
• Application Number: ANDA071523
• Labeler Name: Northwind Pharmaceuticals, LLC
• Substance Name: TRAZODONE HYDROCHLORIDE
• Active Ingredient Strength: 50 mg/1
• Pharm Classes: Serotonin Reuptake Inhibitor [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 51655-634-52

30 TABLET in 1 BOTTLE, DISPENSING (51655-634-52)

• Marketing Start Date: 2014-12-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51655-634-52 [51655063452]

TRAZODONE TABLET

• Marketing Category: ANDA
• Application Number: ANDA071523
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-12-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
TRAZODONE HYDROCHLORIDE	50 mg/1

OpenFDA Data

• SPL SET ID: 17b3356e-458d-47f6-89a5-80828ab48d4c
• Manufacturer:
  • Northwind Pharmaceuticals, LLC
• UNII:
  • 6E8ZO8LRNM
• RxNorm Concept Unique ID - RxCUI:
  • 856377

Pharmacological Class

• Serotonin Reuptake Inhibitor [EPC]

NDC Crossover Matching brand name "TRAZODONE" or generic name "Trazodone"

NDC	Brand Name	Generic Name
51655-634	TRAZODONE	TRAZODONE
21695-133	Trazodone Hydrochloride	Trazodone
21695-134	Trazodone Hydrochloride	Trazodone
21695-135	Trazodone Hydrochloride	Trazodone