Home
>
National Drug Code (NDC)
>
Lyrica
Lyrica - 0071-1020-01 - (PREGABALIN)
Drug Information of Lyrica
| Product NDC: | 0071-1020 |
| Proprietary Name: | Lyrica |
| Non Proprietary Name: | PREGABALIN |
| Active Ingredient(s): | 20 mg/mL & nbsp; PREGABALIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lyrica
| Product NDC: | 0071-1020 |
| Labeler Name: | Parke-Davis Div of Pfizer Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021724 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20041230 |
Package Information of Lyrica
| Package NDC: | 0071-1020-01 |
| Package Description: | 473 mL in 1 BOTTLE (0071-1020-01) |
NDC Information of Lyrica
| NDC Code | 0071-1020-01 |
| Proprietary Name | Lyrica |
| Package Description | 473 mL in 1 BOTTLE (0071-1020-01) |
| Product NDC | 0071-1020 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PREGABALIN |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20041230 |
| Marketing Category Name | NDA |
| Labeler Name | Parke-Davis Div of Pfizer Inc |
| Substance Name | PREGABALIN |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
