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Hydrocodone Bitartrate and Homatropine Methylbromide

NDC 0121-1036, Hydrocodone Bitartrate and Homatropine Methylbromide, solution, from PAI Holdings, LLC dba PAI Pharma.

Product NDC
0121-1036
Status
Listed
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA005213
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0121-1036 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCODONE BITARTRATE5 mg/5mL
  • HOMATROPINE METHYLBROMIDE1.5 mg/5mL

Pharmacologic classes

Opioid Agonist [EPC]; Opioid Agonists [MoA]

Package NDCNDC-11Package
0121-1036-40001211036404 TRAY in 1 CASE (0121-1036-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-1036-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/71319a6f-aaf4-4bc5-8b40-a16c6f139be6

Use it

Look up 0121-1036 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0121-1036 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0121-1036. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.