Lyrica - 63539-013-41 - (PREGABALIN)

Alphabetical Index


Drug Information of Lyrica

Product NDC: 63539-013
Proprietary Name: Lyrica
Non Proprietary Name: PREGABALIN
Active Ingredient(s): 50    mg/1 & nbsp;   PREGABALIN
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Lyrica

Product NDC: 63539-013
Labeler Name: U.S. Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021724
Marketing Category: NDA
Start Marketing Date: 20041230

Package Information of Lyrica

Package NDC: 63539-013-41
Package Description: 1 BLISTER PACK in 1 CARTON (63539-013-41) > 21 CAPSULE in 1 BLISTER PACK

NDC Information of Lyrica

NDC Code 63539-013-41
Proprietary Name Lyrica
Package Description 1 BLISTER PACK in 1 CARTON (63539-013-41) > 21 CAPSULE in 1 BLISTER PACK
Product NDC 63539-013
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PREGABALIN
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20041230
Marketing Category Name NDA
Labeler Name U.S. Pharmaceuticals
Substance Name PREGABALIN
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lyrica


General Information