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Ramelteon

NDC 10135-838, Ramelteon, tablet, film coated, from Marlex Pharmaceuticals, Inc..

Product NDC
10135-838
Status
Listed
Labeler
Marlex Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215435
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10135-838 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RAMELTEON8 mg/1

Pharmacologic classes

Melatonin Receptor Agonist [EPC]; Melatonin Receptor Agonists [MoA]

Package NDCNDC-11Package
10135-838-0110135083801100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10135-838-01)
10135-838-301013508383030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10135-838-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/56d1ac8d-5131-4eed-e063-6294a90a402e

Use it

Look up 10135-838 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10135-838 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10135-838. 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.