Gabapentin

Product NDC
43063-687
11-digit product format
430630687
Labeler code
43063
Product ID
43063-687_7d4f8401-8046-8007-e053-2a91aa0af7be
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
CAPSULE
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA090858
Marketing category
ANDA
Marketing start
2011-01-29
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
43063-687-30EA - Each43063-687dcd771ba-061f-48b4-89ab-d19cb05cf66612017-03-06
43063-687-45EA - Each43063-687f2f7ebc7-7173-40eb-91a6-eb5cbea6b4a012016-09-02
43063-687-60EA - Each43063-6877690e8ce-2c7f-4f81-bc7d-aa6f66a5f5e212017-08-11
43063-687-90EA - Each43063-6875c246d42-5ad3-442b-a7ee-3b5c9efa2b0e12016-10-06