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Pregabalin

NDC 47335-688, Pregabalin, capsule, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-688
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091157
DEA schedule
CV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-688 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREGABALIN75 mg/1
Package NDCNDC-11Package
47335-688-0847335068808100 CAPSULE in 1 BOTTLE (47335-688-08)
47335-688-18473350688181000 CAPSULE in 1 BOTTLE (47335-688-18)
47335-688-834733506888330 CAPSULE in 1 BOTTLE (47335-688-83)
47335-688-8847335068888100 CAPSULE in 1 BOTTLE (47335-688-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ee7b9119-e88f-48ad-ae97-55e53374e62f

Use it

Look up 47335-688 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-688 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-688. 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.