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GABAPENTIN

NDC 76420-836, Gabapentin, tablet, from Asclemed USA, Inc..

Product NDC
76420-836
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214957
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-836 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GABAPENTIN600 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
76420-836-0176420083601100 TABLET in 1 BOTTLE (76420-836-01)
76420-836-0576420083605500 TABLET in 1 BOTTLE (76420-836-05)
76420-836-1276420083612120 TABLET in 1 BOTTLE (76420-836-12)
76420-836-307642008363030 TABLET in 1 BOTTLE (76420-836-30)
76420-836-607642008366060 TABLET in 1 BOTTLE (76420-836-60)
76420-836-907642008369090 TABLET in 1 BOTTLE (76420-836-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1f1203f4-2184-4e13-e063-6394a90a4330

Use it

Look up 76420-836 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-836 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-836. 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.