NDC 68546-177

AUSTEDO

Deutetrabenazine

AUSTEDO is a Kit in the Human Prescription Drug category. It is labeled and distributed by Teva Neuroscience, Inc.. The primary component is .

• Product ID: 68546-177_0de1abef-824f-4d54-9acf-30aa63d87a5a
• NDC: 68546-177
• Product Type: Human Prescription Drug
• Proprietary Name: AUSTEDO
• Generic Name: Deutetrabenazine
• Dosage Form: Kit
• Marketing Start Date: 2020-02-01
• Marketing End Date: 2023-02-28
• Marketing Category: NDA / NDA
• Application Number: NDA208082
• Labeler Name: Teva Neuroscience, Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N

Packaging

NDC 68546-177-21

1 BLISTER PACK in 1 CARTON (68546-177-21) > 1 KIT in 1 BLISTER PACK

• Marketing Start Date: 2020-02-01
• Marketing End Date: 2023-02-28
• NDC Exclude Flag: N
• Sample Package?: Y

NDC SPL Data Element Entries

NDC 68546-177-21 [68546017721]

AUSTEDO KIT

• Marketing Category: NDA
• Application Number: NDA208082
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2020-02-01

Drug Details

OpenFDA Data

• SPL SET ID: 7ea3c60a-45c7-44cc-afc2-d87fa53993c0
• Manufacturer:
  • Teva Neuroscience, Inc.
• UNII:
  • P341G6W9NB
• RxNorm Concept Unique ID - RxCUI:
  • 1876920
  • 1876922
  • 2281115
  • 1876924
  • 1876918
  • 2281116
  • 2281117
  • 2281114
  • 1876916
  • 1876910

NDC Crossover Matching brand name "AUSTEDO" or generic name "Deutetrabenazine"

NDC	Brand Name	Generic Name
68546-170	Austedo	Deutetrabenazine
68546-171	Austedo	Deutetrabenazine
68546-172	Austedo	Deutetrabenazine
68546-176	AUSTEDO	deutetrabenazine
68546-177	AUSTEDO	deutetrabenazine