budesonide
NDC 68682-658, budesonide, aerosol, foam, from Oceanside Pharmaceuticals.
- Product NDC
- 68682-658
- Status
- Listed
- Labeler
- Oceanside Pharmaceuticals
- Dosage form
- AEROSOL, FOAM
- Route
- RECTAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA205613
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68682-658 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BUDESONIDE2 mg/1
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68682-658-03 | 68682065803 | 2 CANISTER in 1 CARTON (68682-658-03) / 1 AEROSOL, FOAM in 1 CANISTER (68682-658-02) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b2cf85c5-3ae0-4f91-9f3a-1d6771e14a73
Use it
Look up 68682-658 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68682-658 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68682-658. 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.