Modafinil

NDC 71205-477, Modafinil, tablet, from Proficient Rx LP.

Product NDC: 71205-477
Status: Listed
Labeler: Proficient Rx LP
Dosage form: TABLET
Route: ORAL
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: ANDA
Application: ANDA202566
DEA schedule: CIV

Request

curl https://api.healthcare.dev/v1/drugs/ndc/71205-477 \
  -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 NDC	NDC-11	Package
71205-477-30	71205047730	30 TABLET in 1 BOTTLE (71205-477-30)
71205-477-60	71205047760	60 TABLET in 1 BOTTLE (71205-477-60)
71205-477-90	71205047790	90 TABLET in 1 BOTTLE (71205-477-90)

Linked data

RxNorm, label and prices

RxNorm concepts

260218modafinil 100 MG Oral Tablet (SCD)

Related lookups

FDA label sections
GET /v1/drugs/labels/ccf7836d-c131-4e7d-a339-fbf99fe7f449

Use it

Look up 71205-477 from code or an agent

curl

curl https://api.healthcare.dev/v1/drugs/ndc/71205-477 \
  -H "Authorization: Bearer $HDEV_API_KEY"

MCP prompt

Using the healthcare.dev MCP server, look up NDC 71205-477. 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.