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Lyrica
Lyrica - 21695-661-90 - (PREGABALIN)
Drug Information of Lyrica
| 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) |
Labeler Information of Lyrica
| 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 Information of Lyrica
| Package NDC: | 21695-661-90 |
| Package Description: | 90 CAPSULE in 1 BOTTLE (21695-661-90) |
NDC Information of Lyrica
| NDC Code | 21695-661-90 |
| Proprietary Name | Lyrica |
| Package Description | 90 CAPSULE in 1 BOTTLE (21695-661-90) |
| 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 |
