Gabapentin — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

GABAPENTIN

Base moiety

GABAPENTIN

RxNorm CUI

310430

UNII

6CW7F3G59X

Medication products

14

Brand names

6

Dosage forms

8

FAERS reports

365,168 · not a risk measure

Products containing this ingredient

Source: NDC Directory 14 products

Gabapentin Powder
37 NDC
Gabapentin Crystal
1 NDC
gabapentin Suspension
Rx NDA TE AA 1 NDC
Gabapentin Capsule
Rx ANDA TE AB 10 recalls 345 NDC
Gabapentin Tablet
Rx ANDA TE AB1 3 recalls 118 NDC
Gabapentin Tablet, Film Coated
Rx ANDA TE AB1 3 recalls 62 NDC
Gabapentin Solution
Rx ANDA TE AA 16 NDC
Gabapentin Tablet, Coated
Rx ANDA TE AB1 21 NDC
GABARONE Gabapentin · Tablet
Rx ANDA TE AB1 2 NDC
Gralise gabapentin · Tablet, Film Coated
Rx NDA TE AB 5 NDC
Neurontin gabapentin · Solution
Rx NDA TE AA 2 NDC
Neurontin gabapentin · Capsule
Rx NDA TE AB 4 NDC
Neurontin gabapentin · Tablet, Film Coated
Rx NDA TE AB1 2 NDC
RELGAABI Gabapentin · Capsule
Rx ANDA TE AB 3 NDC

Entries without a link are products listed by the FDA that carry no approval record, therapeutic equivalence rating or official labelling, so they have no detail page. Their facts are shown inline.

By dosage form

How this ingredient is presented across the catalogue.
Dosage form	Products	Examples
Capsule	3	Gabapentin, Neurontin, RELGAABI
TABLET, Film Coated	3	Gabapentin, Gralise, Neurontin
Tablet	2	Gabapentin, GABARONE
Solution	2	Gabapentin, Neurontin
Powder	1	Gabapentin
Crystal	1	Gabapentin
Suspension	1	gabapentin
TABLET, Coated	1	Gabapentin

Sources for this page

Dataset	Agency	Used for
NDC Directory	FDA	Ingredient name, strengths, products, labelers, packages
DailyMed RxNorm mappings	NLM	RxNorm concept identifier (RxCUI)
FAERS	FDA	Adverse event report totals