NDC 0071-1027

Lyrica CR

Pregabalin

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 ID0071-1027_7ae64cb2-1b1b-456e-8c93-7fc31f0d3113
NDC0071-1027
Product TypeHuman Prescription Drug
Proprietary NameLyrica CR
Generic NamePregabalin
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2018-01-01
Marketing CategoryNDA / NDA
Application NumberNDA209501
Labeler NameParke-Davis Div of Pfizer Inc
Substance NamePREGABALIN
Active Ingredient Strength165 mg/1
DEA ScheduleCV
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0071-1027-01

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0071-1027-01)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0071-1027-01 [00071102701]

Lyrica CR TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA209501
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-01-01

Drug Details

Active Ingredients

IngredientStrength
PREGABALIN165 mg/1

OpenFDA Data

SPL SET ID:2d832165-3d98-497c-84b0-2d9ae3f838f9
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1994389
  • 1994395
  • 1994392
  • 1988980
  • 1988974
  • 1988977
  • UPC Code
  • 0300711027014
  • 0300711026017
  • 0300711029018
  • NDC Crossover Matching brand name "Lyrica CR" or generic name "Pregabalin"

    NDCBrand NameGeneric Name
    0071-1026Lyrica CRLyrica CR
    0071-1027Lyrica CRLyrica CR
    0071-1029Lyrica CRLyrica CR
    63539-024Lyrica CRLyrica CR
    0071-1012LyricaPREGABALIN
    0071-1013LyricaPREGABALIN
    0071-1014LyricaPREGABALIN
    0071-1015LyricaPREGABALIN
    0071-1016LyricaPREGABALIN
    0071-1017LyricaPREGABALIN
    0071-1018LyricaPREGABALIN
    0071-1019LyricaPREGABALIN
    0071-1020LyricaPREGABALIN

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.