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Modafinil

NDC 70771-1051, Modafinil, tablet, from Zydus Lifesciences Limited.

Product NDC
70771-1051
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209966
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1051 \
  -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
70771-1051-170771105101100 TABLET in 1 BOTTLE (70771-1051-1)
70771-1051-37077110510330 TABLET in 1 BOTTLE (70771-1051-3)
70771-1051-97077110510990 TABLET in 1 BOTTLE (70771-1051-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f39820fb-8248-4d42-854c-6fe2d9b92d36

Use it

Look up 70771-1051 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1051 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1051. 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.