Proparacaine Hydrochloride
NDC 70069-601, Proparacaine Hydrochloride, solution/ drops, from Somerset Therapeutics, LLC.
- Product NDC
- 70069-601
- Status
- Listed
- Labeler
- Somerset Therapeutics, LLC
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA215816
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70069-601 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PROPARACAINE HYDROCHLORIDE5 mg/mL
Pharmacologic classes
Local Anesthesia [PE]; Local Anesthetic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70069-601-01 | 70069060101 | 1 BOTTLE in 1 CARTON (70069-601-01) / 15 mL in 1 BOTTLE |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/968a6e4e-814f-41f8-ae22-aa5a82179a6cNADAC price for package 70069060101
GET /v1/drugs/nadac/70069060101
Use it
Look up 70069-601 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70069-601 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70069-601. 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.