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Gabapentin

NDC 16714-332, Gabapentin, tablet, film coated, from NorthStar Rx LLC.

Product NDC
16714-332
Status
Listed
Labeler
NorthStar Rx LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200651
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16714-332 \
  -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
16714-332-0116714033201100 TABLET, FILM COATED in 1 BOTTLE (16714-332-01)
16714-332-0216714033202500 TABLET, FILM COATED in 1 BOTTLE (16714-332-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9508cb1b-3f9f-48bd-8f34-a6fbb68c9a4a

  • NADAC price for package 16714033201

    GET /v1/drugs/nadac/16714033201

  • NADAC price for package 16714033202

    GET /v1/drugs/nadac/16714033202

Use it

Look up 16714-332 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16714-332 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16714-332. 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.