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Gabapentin

NDC 65841-705, Gabapentin, tablet, film coated, from Zydus Lifesciences Limited.

Product NDC
65841-705
Status
Listed
Labeler
Zydus Lifesciences Limited
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/65841-705 \
  -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
65841-705-0165841070501100 TABLET, FILM COATED in 1 BOTTLE (65841-705-01)
65841-705-0565841070505500 TABLET, FILM COATED in 1 BOTTLE (65841-705-05)
65841-705-10658410705101000 TABLET, FILM COATED in 1 BOTTLE (65841-705-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b033c169-4943-4ad9-ace0-7e4a1f0dc100

Use it

Look up 65841-705 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65841-705 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65841-705. 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.