Gabapentin

Product NDC
52343-032
11-digit product format
523430032
Labeler code
52343
Product ID
52343-032_19e835f7-2223-4d65-a702-70176cd1c9c7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
CAPSULE
Route
ORAL
Labeler
ACETRIS HEALTH, LLC
Application
ANDA078787
Marketing category
ANDA
Marketing start
2008-01-31
Marketing end
2020-09-01
Substance
GABAPENTIN
Active strength
400 mg/1
Pharmacologic classes
Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
52343-032-01EA - Each52343-0326b48808c-f113-496f-ba52-05b9eb2a7b7c12013-08-02
52343-032-05EA - Each52343-03200237c99-953d-458c-9e35-1e60ca5341bf12013-08-02
52343-032-27EA - Each52343-0323c319433-9367-4996-87fa-07315881abf412013-08-02
52343-032-90EA - Each52343-032b52d8151-80ea-48eb-9320-5624f3a5eaa512013-08-02