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Modafinil

NDC 46708-385, Modafinil, tablet, from Alembic Pharmaceuticals Limited.

Product NDC
46708-385
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202700
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/46708-385 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MODAFINIL100 mg/1

Pharmacologic classes

Central Nervous System Stimulation [PE]; Increased Sympathetic Activity [PE]; Sympathomimetic-like Agent [EPC]

Package NDCNDC-11Package
46708-385-1046708038510100 TABLET in 1 CARTON (46708-385-10)
46708-385-304670803853030 TABLET in 1 BOTTLE (46708-385-30)
46708-385-604670803856060 TABLET in 1 BOTTLE (46708-385-60)
46708-385-904670803859090 TABLET in 1 BOTTLE (46708-385-90)
46708-385-91467080385911000 TABLET in 1 BOTTLE (46708-385-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5b8496fe-b647-4ce6-aeef-71245712e46f

Use it

Look up 46708-385 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-385 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-385. 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.