Pregabalin

Product NDC
68788-8667
11-digit product format
687888667
Labeler code
68788
Product ID
68788-8667_e47d9514-bb38-42b4-bbd8-1913d4f9060d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pregabalin
Dosage form
CAPSULE
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA206912
Marketing category
ANDA
Marketing start
2024-05-17
Substance
PREGABALIN
Active strength
150 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
68788-8667-168788866701100 CAPSULE in 1 BOTTLE (68788-8667-1) 100 capsule2024-05-17NoNoHistorical
68788-8667-36878886670330 CAPSULE in 1 BOTTLE (68788-8667-3) 30 capsule2024-05-17NoNoHistorical
68788-8667-66878886670660 CAPSULE in 1 BOTTLE (68788-8667-6) 60 capsule2024-05-17NoNoHistorical
68788-8667-96878886670990 CAPSULE in 1 BOTTLE (68788-8667-9) 90 capsule2024-05-17NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PregabalinPreferred Pharmaceuticals Inc.2025-09-15HUMAN PRESCRIPTION DRUG LABEL2