Gabapentin

Product NDC
50268-348
11-digit product format
502680348
Labeler code
50268
Product ID
50268-348_64b883d0-ef40-651d-e053-2a91aa0a3f40
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
GABAPENTIN
Dosage form
CAPSULE
Route
ORAL
Labeler
AvPAK
Application
ANDA090007
Marketing category
ANDA
Marketing start
2016-03-10
Marketing end
0000-00-00
Substance
GABAPENTIN
Active strength
300 mg/1
Pharmacologic classes
Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50268-348-11EA - Each50268-3486813ed99-4eab-41f4-ad63-4df9f32cebdb12016-03-04
50268-348-15EA - Each50268-348a67d995e-988d-4cf4-ace4-957be7a953ef12016-02-04