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Gabapentin

NDC 71205-514, Gabapentin, tablet, from Proficient Rx LP.

Product NDC
71205-514
Status
Listed
Labeler
Proficient Rx LP
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/71205-514 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GABAPENTIN800 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71205-514-307120505143030 TABLET in 1 BOTTLE (71205-514-30)
71205-514-607120505146060 TABLET in 1 BOTTLE (71205-514-60)
71205-514-907120505149090 TABLET in 1 BOTTLE (71205-514-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2b76955c-52a4-4026-b286-3da1112fe989

Use it

Look up 71205-514 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-514 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-514. 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.