Home
>
National Drug Code (NDC)
>
Lyrica
Lyrica - 54868-6063-1 - (pregabalin)
Drug Information of Lyrica
| Product NDC: | 54868-6063 |
| Proprietary Name: | Lyrica |
| Non Proprietary Name: | pregabalin |
| Active Ingredient(s): | 200 mg/1 & nbsp; pregabalin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lyrica
| Product NDC: | 54868-6063 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021724 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20090904 |
Package Information of Lyrica
| Package NDC: | 54868-6063-1 |
| Package Description: | 90 CAPSULE in 1 BOTTLE (54868-6063-1) |
NDC Information of Lyrica
| NDC Code | 54868-6063-1 |
| Proprietary Name | Lyrica |
| Package Description | 90 CAPSULE in 1 BOTTLE (54868-6063-1) |
| Product NDC | 54868-6063 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | pregabalin |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20090904 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | PREGABALIN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
