GABAPENTIN

Product NDC
60760-039
11-digit product format
607600039
Labeler code
60760
Product ID
60760-039_7a8e8601-c88e-a477-e053-2a91aa0ab8f6
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
GABAPENTIN
Dosage form
CAPSULE
Route
ORAL
Labeler
St.Mary's Medical Park Pharmacy
Application
ANDA090705
Marketing category
ANDA
Marketing start
2016-06-29
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
60760-039-30EA - Each60760-03960626cf3-1953-40a5-a1d0-8bb671bfeeda12017-06-15
60760-039-60EA - Each60760-039cb1f9bbf-7951-4491-80af-e83ed8db1bcf12017-06-15
60760-039-90EA - Each60760-039aa06fdac-446a-43d0-b3b0-50cd67117fcb12017-06-15
60760-039-92EA - Each60760-039250b5358-651d-48d0-a7c4-6d5ba04f125b12017-12-14