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GABAPENTIN

NDC 85509-1166, Gabapentin, tablet, from PHOENIX RX LLC.

Product NDC
85509-1166
Status
Listed
Labeler
PHOENIX RX LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214957
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1166 \
  -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
85509-1166-38550911660330 TABLET in 1 BOTTLE (85509-1166-3)
85509-1166-68550911660660 TABLET in 1 BOTTLE (85509-1166-6)
85509-1166-98550911660990 TABLET in 1 BOTTLE (85509-1166-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5a85ea98-4211-54eb-e063-6294a90aff33

Use it

Look up 85509-1166 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1166 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85509-1166. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.