Pregabalin

Product NDC
71335-1762
11-digit product format
713351762
Labeler code
71335
Product ID
71335-1762_fc5da7ff-458b-46c8-81f5-a09045bd19e4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pregabalin
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA207799
Marketing category
ANDA
Marketing start
2019-10-02
Substance
PREGABALIN
Active strength
25 mg/1
DEA schedule
CV
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Pregabalin
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PREGABALIN25 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii55JG375S6M
Rxcui483442

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1762-17133517620130 CAPSULE in 1 BOTTLE (71335-1762-1) 30 capsule2024-09-060000-00-00NoNoCurrent
71335-1762-27133517620260 CAPSULE in 1 BOTTLE (71335-1762-2) 60 capsule2021-10-250000-00-00NoNoCurrent
71335-1762-37133517620390 CAPSULE in 1 BOTTLE (71335-1762-3) 90 capsule2021-01-190000-00-00NoNoCurrent
71335-1762-47133517620415 CAPSULE in 1 BOTTLE (71335-1762-4) 15 capsule2024-09-06NoNoHistorical