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HYDROMORPHONE HYDROCHLORIDE

NDC 13107-108, HYDROMORPHONE HYDROCHLORIDE, tablet, from Aurolife Pharma, LLC.

Product NDC
13107-108
Status
Listed
Labeler
Aurolife Pharma, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205814
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/13107-108 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROMORPHONE HYDROCHLORIDE4 mg/1

Pharmacologic classes

Full Opioid Agonists [MoA]; Opioid Agonist [EPC]

Package NDCNDC-11Package
13107-108-0113107010801100 TABLET in 1 BOTTLE (13107-108-01)
13107-108-0513107010805500 TABLET in 1 BOTTLE (13107-108-05)
13107-108-201310701082020 TABLET in 1 BOTTLE (13107-108-20)
13107-108-99131070108991000 TABLET in 1 BOTTLE (13107-108-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f778dfab-e109-428e-b1b7-4dfb1b8293e4

  • NADAC price for package 13107010801

    GET /v1/drugs/nadac/13107010801

Use it

Look up 13107-108 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/13107-108 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 13107-108. 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.