Home > National Drug Code (NDC) > Carisoprodol

Carisoprodol - 35356-721-10 - (Carisoprodol)

Alphabetical Index


Drug Information of Carisoprodol

Product NDC: 35356-721
Proprietary Name: Carisoprodol
Non Proprietary Name: Carisoprodol
Active Ingredient(s): 350    mg/1 & nbsp;   Carisoprodol
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Carisoprodol

Product NDC: 35356-721
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087499
Marketing Category: ANDA
Start Marketing Date: 19871101

Package Information of Carisoprodol

Package NDC: 35356-721-10
Package Description: 10 TABLET in 1 BOTTLE (35356-721-10)

NDC Information of Carisoprodol

NDC Code 35356-721-10
Proprietary Name Carisoprodol
Package Description 10 TABLET in 1 BOTTLE (35356-721-10)
Product NDC 35356-721
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carisoprodol
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19871101
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name CARISOPRODOL
Strength Number 350
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Carisoprodol


General Information