Pregabalin

Product NDC
80425-0308
11-digit product format
804250308
Labeler code
80425
Product ID
80425-0308_2a9bfe6a-6d6a-b262-e063-6294a90a1cf3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pregabalin
Dosage form
CAPSULE
Route
ORAL
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Application
ANDA208677
Marketing category
ANDA
Marketing start
2023-04-06
Substance
PREGABALIN
Active strength
200 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
80425-0308-18042503080130 CAPSULE in 1 BOTTLE (80425-0308-1) 30 capsule2023-04-06NoNoHistorical
80425-0308-28042503080260 CAPSULE in 1 BOTTLE (80425-0308-2) 60 capsule2023-04-06NoNoHistorical
80425-0308-38042503080390 CAPSULE in 1 BOTTLE (80425-0308-3) 90 capsule2023-04-06NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Pregabalin CapsulesAdvanced Rx Pharmacy of Tennessee, LLC2024-12-31HUMAN PRESCRIPTION DRUG LABEL2