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Gabapentin

NDC 76420-235, Gabapentin, tablet, from Asclemed USA, Inc..

Product NDC
76420-235
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205101
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-235 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GABAPENTIN600 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC]; Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
76420-235-1276420023512120 TABLET in 1 BOTTLE (76420-235-12)
76420-235-2476420023524240 TABLET in 1 BOTTLE (76420-235-24)
76420-235-307642002353030 TABLET in 1 BOTTLE (76420-235-30)
76420-235-607642002356060 TABLET in 1 BOTTLE (76420-235-60)
76420-235-907642002359090 TABLET in 1 BOTTLE (76420-235-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c18d9d06-f796-4eb7-8fd5-1de4ebb95439

Use it

Look up 76420-235 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-235 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-235. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.