PULMICORT RESPULES
NDC 0186-1988, Budesonide, suspension, from AstraZeneca Pharmaceuticals LP.
- Product NDC
- 0186-1988
- Status
- Listed
- Labeler
- AstraZeneca Pharmaceuticals LP
- Dosage form
- SUSPENSION
- Route
- RESPIRATORY (INHALATION)
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA020929
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0186-1988 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BUDESONIDE.25 mg/2mL
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0186-1988-04 | 00186198804 | 6 POUCH in 1 CARTON (0186-1988-04) / 5 AMPULE in 1 POUCH / 2 mL in 1 AMPULE |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/33cd9834-76df-4f26-3fa2-aab6b9eee8f2Medicare Part B payment limits (ASP)
GET /v1/drugs/asp?ndc=0186-1988
Use it
Look up 0186-1988 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0186-1988 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0186-1988. 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.