GABAPENTIN- gabapentin capsule 
NuCare Pharmaceuticals, Inc.

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HOW SUPPLIED

300 mg Capsules (Yellow/Yellow colored, size '1' hard gelatin capsules with "104" printed on body of capsules containing white to off white granular powder Bottles of 7 NDC 68071-3230-7

Bottles of 14 NDC 68071-3230-5

Bottles of 30 NDC 68071-3230-3

Bottles of 60 NDC 68071-3230-6

Bottles of 84 NDC 68071-3230-4

Bottles of 90 NDC 68071-3230-9

Bottles of 120 NDC 68071-3230-1

Bottles of 180 NDC 68071-3230-8

Bottles of 270 NDC 68071-3230-2

300mg Gabapentin Capsule Package Label

pdp

GABAPENTIN 
gabapentin capsule
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:68071-3230(NDC:49483-606)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GABAPENTIN (UNII: 6CW7F3G59X) (GABAPENTIN - UNII:6CW7F3G59X) GABAPENTIN300 mg
Inactive Ingredients
Ingredient NameStrength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
STARCH, CORN (UNII: O8232NY3SJ)  
TALC (UNII: 7SEV7J4R1U)  
GELATIN (UNII: 2G86QN327L)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SHELLAC (UNII: 46N107B71O)  
Product Characteristics
ColoryellowScoreno score
ShapeCAPSULESize19mm
FlavorImprint Code 104
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68071-3230-77 in 1 BOTTLE; Type 0: Not a Combination Product05/19/2017
2NDC:68071-3230-514 in 1 BOTTLE; Type 0: Not a Combination Product05/19/2017
3NDC:68071-3230-330 in 1 BOTTLE; Type 0: Not a Combination Product05/19/2017
4NDC:68071-3230-660 in 1 BOTTLE; Type 0: Not a Combination Product05/19/2017
5NDC:68071-3230-484 in 1 BOTTLE; Type 0: Not a Combination Product05/19/2017
6NDC:68071-3230-990 in 1 BOTTLE; Type 0: Not a Combination Product05/19/2017
7NDC:68071-3230-1120 in 1 BOTTLE; Type 0: Not a Combination Product05/19/2017
8NDC:68071-3230-8180 in 1 BOTTLE; Type 0: Not a Combination Product05/19/2017
9NDC:68071-3230-2270 in 1 BOTTLE; Type 0: Not a Combination Product05/19/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA09000712/30/2015
Labeler - NuCare Pharmaceuticals, Inc. (010632300)
Establishment
NameAddressID/FEIBusiness Operations
NuCare Pharmaceuticals, Inc.010632300repack(68071-3230)

Revised: 2/2021
Document Id: bafe10da-e52e-55fd-e053-2995a90ad011
Set id: 4fe85b34-8fe8-56fa-e054-00144ff88e88
Version: 3
Effective Time: 20210210
 
NuCare Pharmaceuticals, Inc.