Product NDC: | 23155-128 |
Proprietary Name: | Meprobamate |
Non Proprietary Name: | Meprobamate |
Active Ingredient(s): | 200 mg/1 & nbsp; Meprobamate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 23155-128 |
Labeler Name: | Heritage Pharmaceuticals Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090122 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090624 |
Package NDC: | 23155-128-03 |
Package Description: | 30 TABLET in 1 BOTTLE (23155-128-03) |
NDC Code | 23155-128-03 |
Proprietary Name | Meprobamate |
Package Description | 30 TABLET in 1 BOTTLE (23155-128-03) |
Product NDC | 23155-128 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Meprobamate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20090624 |
Marketing Category Name | ANDA |
Labeler Name | Heritage Pharmaceuticals Inc |
Substance Name | MEPROBAMATE |
Strength Number | 200 |
Strength Unit | mg/1 |
Pharmaceutical Classes |