Product NDC: | 35356-734 |
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) |
Product NDC: | 35356-734 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040124 |
Marketing Category: | ANDA |
Start Marketing Date: | 19960124 |
Package NDC: | 35356-734-14 |
Package Description: | 14 TABLET in 1 BOTTLE, PLASTIC (35356-734-14) |
NDC Code | 35356-734-14 |
Proprietary Name | Carisoprodol |
Package Description | 14 TABLET in 1 BOTTLE, PLASTIC (35356-734-14) |
Product NDC | 35356-734 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Carisoprodol |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19960124 |
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] |