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NDC 00115-1012-08 Baclofen 20 mg/1 Details

Baclofen 20 mg/1

Baclofen is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals of New York LLC. The primary component is BACLOFEN.

MedlinePlus Drug Summary

Baclofen is used to treat pain and certain types of spasticity (muscle stiffness and tightness) from multiple sclerosis, spinal cord injuries, or other spinal cord diseases. Baclofen is in a class of medications called skeletal muscle relaxants. Baclofen acts on the spinal cord nerves and decreases the number and severity of muscle spasms caused by multiple sclerosis or spinal cord conditions. It also relieves pain and improves muscle movement.

Related Packages: 00115-1012-08
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Baclofen

Product Information

NDC	00115-1012
Product ID	0115-1012_e73c54db-d445-4784-9553-4e04fe9163ca
Associated GPIs	75100010000310
GCN Sequence Number	004680
GCN Sequence Number Description	baclofen TABLET 20 MG ORAL
HIC3	H6H
HIC3 Description	SKELETAL MUSCLE RELAXANTS
GCN	18011
HICL Sequence Number	001949
HICL Sequence Number Description	BACLOFEN
Brand/Generic	Generic
Proprietary Name	Baclofen
Proprietary Name Suffix	n/a
Non-Proprietary Name	Baclofen
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	20
Active Ingredient Units	mg/1
Substance Name	BACLOFEN
Labeler Name	Amneal Pharmaceuticals of New York LLC
Pharmaceutical Class	GABA A Agonists [MoA], GABA B Agonists [MoA], gamma-Aminobutyric Acid-ergic Agonist [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA077971
Listing Certified Through	2024-12-31

Package

NDC 00115-1012-08 (00115101208)

Pricing Information	N/A
NDC Package Code	0115-1012-08
Billing NDC	00115101208
Package	30 TABLET in 1 BOTTLE (0115-1012-08)
Marketing Start Date	2007-10-27
NDC Exclude Flag	N