Tretinoin
NDC 69238-2323, Tretinoin, gel, from Amneal Pharmaceuticals NY LLC.
- Product NDC
- 69238-2323
- Status
- Listed
- Labeler
- Amneal Pharmaceuticals NY LLC
- Dosage form
- GEL
- Route
- TOPICAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA217497
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/69238-2323 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- TRETINOIN.8 mg/g
Pharmacologic classes
Retinoid [EPC]; Retinoids [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 69238-2323-1 | 69238232301 | 1 BOTTLE, PUMP in 1 CARTON (69238-2323-1) / 50 g in 1 BOTTLE, PUMP |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/4b6006e3-f7a4-4823-8217-3e5b0f7e58d9
Use it
Look up 69238-2323 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/69238-2323 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 69238-2323. 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.