Product NDC: | 21695-661 |
Proprietary Name: | Lyrica |
Non Proprietary Name: | PREGABALIN |
Active Ingredient(s): | 100 mg/1 & nbsp; PREGABALIN |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-661 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021724 |
Marketing Category: | NDA |
Start Marketing Date: | 20050610 |
Package NDC: | 21695-661-60 |
Package Description: | 60 CAPSULE in 1 BOTTLE (21695-661-60) |
NDC Code | 21695-661-60 |
Proprietary Name | Lyrica |
Package Description | 60 CAPSULE in 1 BOTTLE (21695-661-60) |
Product NDC | 21695-661 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | PREGABALIN |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20050610 |
Marketing Category Name | NDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | PREGABALIN |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes |