NDC 73289-0002

VIGADRONE

Vigabatrin

VIGADRONE is a Oral Powder, For Solution in the Human Prescription Drug category. It is labeled and distributed by Aucta Pharmaceuticals, Inc.. The primary component is Vigabatrin.

• Product ID: 73289-0002_dd044b83-e2c9-66e8-e053-2a95a90aa3fd
• NDC: 73289-0002
• Product Type: Human Prescription Drug
• Proprietary Name: VIGADRONE
• Generic Name: Vigabatrin
• Dosage Form: Powder, For Solution
• Route of Administration: ORAL
• Marketing Start Date: 2018-06-21
• Marketing Category: ANDA /
• Application Number: ANDA210196
• Labeler Name: Aucta Pharmaceuticals, Inc.
• Substance Name: VIGABATRIN
• Active Ingredient Strength: 50 mg/mL
• Pharm Classes: Anti-epileptic Agent [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 73289-0002-0

50 PACKAGE in 1 CARTON (73289-0002-0) > 10 mL in 1 PACKAGE

• Marketing Start Date: 2018-06-21
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "VIGADRONE" or generic name "Vigabatrin"

NDC	Brand Name	Generic Name
0245-0556	VIGADRONE	vigabatrin
67386-111	SABRIL	vigabatrin
67386-211	SABRIL	vigabatrin
0054-0652	Vigabatrin	Vigabatrin
0574-0201	VIGABATRIN	vigabatrin
0574-0470	VIGABATRIN	vigabatrin
0591-3851	Vigabatrin	Vigabatrin
0591-3955	vigabatrin	vigabatrin
16729-521	Vigabatrin	Vigabatrin
42799-950	Vigabatrin	Vigabatrin
43598-651	Vigabatrin	Vigabatrin
43598-697	Vigabatrin	Vigabatrin
49884-358	VIGABATRIN	vigabatrin
59651-366	Vigabatrin	Vigabatrin
59651-367	Vigabatrin	Vigabatrin
64850-940	Vigabatrin	vigabatrin
31722-009	vigabatrin for oral solution	vigabatrin
0054-0702	Vigabatrin for oral solution USP, 500 mg	Vigabatrin