FLUTICASONE PROPIONATE
NDC 68071-3949, FLUTICASONE PROPIONATE, spray, from NuCare Pharmaceuticals, Inc..
- Product NDC
- 68071-3949
- Status
- Listed
- Labeler
- NuCare Pharmaceuticals, Inc.
- Dosage form
- SPRAY
- Route
- NASAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA218321
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3949 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FLUTICASONE PROPIONATE50 ug/1
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68071-3949-5 | 68071394905 | 1 BOTTLE, SPRAY in 1 CARTON (68071-3949-5) / 120 SPRAY in 1 BOTTLE, SPRAY |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/4849c4e5-58ea-972c-e063-6394a90a809c
Use it
Look up 68071-3949 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3949 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68071-3949. 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.