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NDC 00054-0702-19 Vigabatrin for oral solution USP, 500 mg 50 mg/mL Details

Vigabatrin for oral solution USP, 500 mg 50 mg/mL

Vigabatrin for oral solution USP, 500 mg is a ORAL FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Hikma Pharmaceuticals USA Inc.. The primary component is VIGABATRIN.

MedlinePlus Drug Summary

Vigabatrin tablets are used in combination with other medications to control certain types of seizures in adults and children 10 years of age or older whose seizures were not controlled by several other medications. Vigabatrin powder is used to control infantile spasms (a type of seizure that babies and children can have) in babies 1 month to 2 years of age. Vigabatrin is in a class of medications called anticonvulsants. It works by decreasing abnormal electrical activity in the brain.

Related Packages: 00054-0702-19
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Vigabatrin

Product Information

NDC	00054-0702
Product ID	0054-0702_f4cea32f-ca86-ce64-e053-2995a90a3cd1
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Vigabatrin for oral solution USP, 500 mg
Proprietary Name Suffix	n/a
Non-Proprietary Name	Vigabatrin
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	FOR SOLUTION
Route	ORAL
Active Ingredient Strength	50
Active Ingredient Units	mg/mL
Substance Name	VIGABATRIN
Labeler Name	Hikma Pharmaceuticals USA Inc.
Pharmaceutical Class	Anti-epileptic Agent [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA213469
Listing Certified Through	2024-12-31

Package

NDC 00054-0702-19 (00054070219)

Pricing Information	N/A
NDC Package Code	0054-0702-19
Billing NDC	00054070219
Package	50 PACKET in 1 CARTON (0054-0702-19) / 10 mL in 1 PACKET
Marketing Start Date	2020-07-10
NDC Exclude Flag	N