Product NDC: | 35356-303 |
Proprietary Name: | Prandin |
Non Proprietary Name: | Repaglinide |
Active Ingredient(s): | .5 mg/1 & nbsp; Repaglinide |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35356-303 |
Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020741 |
Marketing Category: | NDA |
Start Marketing Date: | 20101012 |
Package NDC: | 35356-303-01 |
Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (35356-303-01) |
NDC Code | 35356-303-01 |
Proprietary Name | Prandin |
Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (35356-303-01) |
Product NDC | 35356-303 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Repaglinide |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20101012 |
Marketing Category Name | NDA |
Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | REPAGLINIDE |
Strength Number | .5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Glinide [EPC],Potassium Channel Antagonists [MoA] |