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Ramelteon

NDC 72319-005, Ramelteon, tablet, film coated, from i3 Pharmaceuticals, LLC.

Product NDC
72319-005
Status
Listed
Labeler
i3 Pharmaceuticals, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212650
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72319-005 \
  -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
72319-005-017231900050130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72319-005-01)
72319-005-0472319000504100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72319-005-04)
72319-005-0572319000505500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72319-005-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/32c52e03-4c2e-4774-9397-f1f0ee99b320

Use it

Look up 72319-005 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72319-005 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72319-005. 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.