Modafinil

NDC 71205-544, Modafinil, tablet, from Proficient Rx LP.

Product NDC: 71205-544
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/71205-544 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

MODAFINIL200 mg/1

Pharmacologic classes

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

Package NDC	NDC-11	Package
71205-544-30	71205054430	30 TABLET in 1 BOTTLE (71205-544-30)
71205-544-60	71205054460	60 TABLET in 1 BOTTLE (71205-544-60)
71205-544-90	71205054490	90 TABLET in 1 BOTTLE (71205-544-90)

Linked data

RxNorm, label and prices

RxNorm concepts

205324modafinil 200 MG Oral Tablet (SCD)

Related lookups

FDA label sections
GET /v1/drugs/labels/d97684d7-c236-451e-99bd-b8df4bf36643

Use it

Look up 71205-544 from code or an agent

curl

curl https://api.healthcare.dev/v1/drugs/ndc/71205-544 \
  -H "Authorization: Bearer $HDEV_API_KEY"

MCP prompt

Using the healthcare.dev MCP server, look up NDC 71205-544. 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.