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gabapentin

NDC 68382-356, gabapentin, tablet, from Zydus Pharmaceuticals USA Inc..

Product NDC
68382-356
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203934
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68382-356 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GABAPENTIN750 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
68382-356-0168382035601100 TABLET in 1 BOTTLE (68382-356-01)
68382-356-146838203561460 TABLET in 1 BOTTLE (68382-356-14)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3cfd04ab-e421-441f-a10e-e4dd1412974d

Use it

Look up 68382-356 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-356 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-356. 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.