Condylox
NDC 0023-6118, podofilox, gel, from Allergan, Inc..
- Product NDC
- 0023-6118
- Status
- Listed
- Labeler
- Allergan, Inc.
- Dosage form
- GEL
- Route
- TOPICAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA020529
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0023-6118 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PODOFILOX5 mg/g
Pharmacologic classes
Decreased Mitosis [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0023-6118-03 | 00023611803 | 3.5 g in 1 TUBE, WITH APPLICATOR (0023-6118-03) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/032e4bcb-b1ed-4029-b2a6-e92f3bf5cc37
Use it
Look up 0023-6118 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0023-6118 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0023-6118. 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.