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Gabapentin

NDC 68382-204, Gabapentin, tablet, film coated, from Zydus Pharmaceuticals USA Inc..

Product NDC
68382-204
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078926
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68382-204 \
  -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
68382-204-0168382020401100 TABLET, FILM COATED in 1 BOTTLE (68382-204-01)
68382-204-0568382020405500 TABLET, FILM COATED in 1 BOTTLE (68382-204-05)
68382-204-10683820204101000 TABLET, FILM COATED in 1 BOTTLE (68382-204-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/310ce005-5a24-489a-b23c-d42ab6a3bfed

  • NADAC price for package 68382020401

    GET /v1/drugs/nadac/68382020401

  • NADAC price for package 68382020405

    GET /v1/drugs/nadac/68382020405

Use it

Look up 68382-204 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-204 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-204. 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.