Gabapentin

Product NDC
42291-300
11-digit product format
422910300
Labeler code
42291
Product ID
42291-300_7354472d-acb4-4817-e053-2a91aa0a08c6
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
CAPSULE
Route
ORAL
Labeler
AvKARE, Inc.
Application
ANDA078428
Marketing category
ANDA
Marketing start
2018-08-15
Marketing end
0000-00-00
Substance
GABAPENTIN
Active strength
100 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
42291-300-10EA - Each42291-3005c2871aa-905f-41a6-bbd1-b1d511795efb12013-02-13
42291-300-18EA - Each42291-300f93a8097-a3fc-4094-9928-1d8dc1f4b3ff12013-02-13
42291-300-27EA - Each42291-300bbdabb19-ab3b-431f-bd23-0835bfba9a6412013-02-13
42291-300-50EA - Each42291-3004cd07640-6393-40d1-a357-e3afd2c2a6af12018-10-11
42291-300-90EA - Each42291-3000243b5bf-5396-4442-8e56-5f5cd79a41e212013-02-13