Pregabalin

Product NDC
71205-870
11-digit product format
712050870
Labeler code
71205
Product ID
71205-870_1815296c-fc89-41c8-9079-ffb947b59b0f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pregabalin
Dosage form
CAPSULE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA208677
Marketing category
ANDA
Marketing start
2021-08-24
Substance
PREGABALIN
Active strength
50 mg/1
DEA schedule
CV
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
55JG375S6MPREGABALIN148553-50-8PREGABALIN

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71205-870-0071205087000100 CAPSULE in 1 BOTTLE (71205-870-00) 100 capsule2021-12-21NoNoHistorical
71205-870-11712050870111000 CAPSULE in 1 BOTTLE (71205-870-11) 1000 capsule2021-12-21NoNoHistorical
71205-870-307120508703030 CAPSULE in 1 BOTTLE (71205-870-30) 30 capsule2021-12-21NoNoHistorical
71205-870-5571205087055500 CAPSULE in 1 BOTTLE (71205-870-55) 500 capsule2021-12-21NoNoHistorical
71205-870-607120508706060 CAPSULE in 1 BOTTLE (71205-870-60) 60 capsule2021-12-21NoNoHistorical
71205-870-6771205087067270 CAPSULE in 1 BOTTLE (71205-870-67) 270 capsule2021-12-21NoNoHistorical
71205-870-7271205087072120 CAPSULE in 1 BOTTLE (71205-870-72) 120 capsule2021-12-21NoNoHistorical
71205-870-7871205087078180 CAPSULE in 1 BOTTLE (71205-870-78) 180 capsule2021-12-21NoNoHistorical
71205-870-907120508709090 CAPSULE in 1 BOTTLE (71205-870-90) 90 capsule2021-12-21NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PregabalinAphena Pharma Solutions - Tennessee, LLC2024-04-12HUMAN PRESCRIPTION DRUG LABEL1
PregabalinProficient Rx LP2022-04-01HUMAN PRESCRIPTION DRUG LABEL2