NDC 0008-4117

Trecator

Ethionamide

Trecator is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Wyeth Pharmaceuticals Llc, A Subsidiary Of Pfizer Inc.. The primary component is Ethionamide.

• Product ID: 0008-4117_3f9c1f21-bc27-434c-93d0-b40837391c78
• NDC: 0008-4117
• Product Type: Human Prescription Drug
• Proprietary Name: Trecator
• Generic Name: Ethionamide
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2004-11-08
• Marketing Category: NDA / NDA
• Application Number: NDA013026
• Labeler Name: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
• Substance Name: ETHIONAMIDE
• Active Ingredient Strength: 250 mg/1
• Pharm Classes: Antimycobacterial [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0008-4117-01

100 TABLET, FILM COATED in 1 BOTTLE (0008-4117-01)

• Marketing Start Date: 2004-11-08
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0008-4117-01 [00008411701]

Trecator TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA013026
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2004-11-08

Drug Details

Active Ingredients

Ingredient	Strength
ETHIONAMIDE	250 mg/1

OpenFDA Data

• SPL SET ID: 04a413fe-95f4-47a7-42ac-283a9e78297d
• Manufacturer:
  • Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc.
• UNII:
  • OAY8ORS3CQ
• RxNorm Concept Unique ID - RxCUI:
  • 197681
  • 835721

Pharmacological Class

• Antimycobacterial [EPC]