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Gabapentin

NDC 82619-146, Gabapentin, tablet, from Creekwood Pharmaceuticals LLC.

Product NDC
82619-146
Status
Listed
Labeler
Creekwood Pharmaceuticals LLC
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/82619-146 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GABAPENTIN800 mg/1

Pharmacologic classes

Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
82619-146-0182619014601100 TABLET in 1 BOTTLE (82619-146-01)
82619-146-0282619014602500 TABLET in 1 BOTTLE (82619-146-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/266ef369-0a56-f225-e063-6294a90a495e

Use it

Look up 82619-146 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82619-146 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82619-146. 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.