GABAPENTIN

Product NDC
43063-776
11-digit product format
430630776
Labeler code
43063
Product ID
43063-776_7d50d864-ac47-c66f-e053-2991aa0a2424
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
GABAPENTIN
Dosage form
TABLET
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA205101
Marketing category
ANDA
Marketing start
2016-11-20
Marketing end
0000-00-00
Substance
GABAPENTIN
Active strength
600 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
43063-776-30EA - Each43063-77674a92fb7-7c6d-463d-8da4-abea9bcbc90112017-09-11
43063-776-60EA - Each43063-776c9a93693-f561-48ff-8d47-ac8d6ef197b712017-09-11
43063-776-90EA - Each43063-776fff83614-5f9e-4394-ada9-097ff78312e112017-09-11