Lyrica CR is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Parke-davis Div Of Pfizer Inc. The primary component is Pregabalin.
Product ID | 0071-1029_7ae64cb2-1b1b-456e-8c93-7fc31f0d3113 |
NDC | 0071-1029 |
Product Type | Human Prescription Drug |
Proprietary Name | Lyrica CR |
Generic Name | Pregabalin |
Dosage Form | Tablet, Film Coated, Extended Release |
Route of Administration | ORAL |
Marketing Start Date | 2018-01-01 |
Marketing Category | NDA / NDA |
Application Number | NDA209501 |
Labeler Name | Parke-Davis Div of Pfizer Inc |
Substance Name | PREGABALIN |
Active Ingredient Strength | 330 mg/1 |
DEA Schedule | CV |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2018-01-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA209501 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2018-01-01 |
Ingredient | Strength |
---|---|
PREGABALIN | 330 mg/1 |
SPL SET ID: | 2d832165-3d98-497c-84b0-2d9ae3f838f9 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
0071-1026 | Lyrica CR | Lyrica CR |
0071-1027 | Lyrica CR | Lyrica CR |
0071-1029 | Lyrica CR | Lyrica CR |
63539-024 | Lyrica CR | Lyrica CR |
0071-1012 | Lyrica | PREGABALIN |
0071-1013 | Lyrica | PREGABALIN |
0071-1014 | Lyrica | PREGABALIN |
0071-1015 | Lyrica | PREGABALIN |
0071-1016 | Lyrica | PREGABALIN |
0071-1017 | Lyrica | PREGABALIN |
0071-1018 | Lyrica | PREGABALIN |
0071-1019 | Lyrica | PREGABALIN |
0071-1020 | Lyrica | PREGABALIN |