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
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 NDC | NDC-11 | Package |
|---|---|---|
| 0121-1036-40 | 00121103640 | 4 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 https://api.healthcare.dev/v1/drugs/ndc/0121-1036 \ -H "Authorization: Bearer $HDEV_API_KEY"
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.