Albuterol Sulfate
NDC 17270-0740, Albuterol Sulfate, inhalant, from Armstrong Pharmaceuticals, Inc..
- Product NDC
- 17270-0740
- Status
- Listed
- Labeler
- Armstrong Pharmaceuticals, Inc.
- Dosage form
- INHALANT
- Route
- RESPIRATORY (INHALATION)
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA212447
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/17270-0740 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ALBUTEROL SULFATE90 ug/1
Pharmacologic classes
Adrenergic beta2-Agonists [MoA]; beta2-Adrenergic Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 17270-0740-0 | 17270074000 | 1 INHALER in 1 CARTON (17270-0740-0) / 200 INHALANT in 1 INHALER |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/17858afa-dcdf-4612-b475-3b6baadfb639NADAC price for package 17270074000
GET /v1/drugs/nadac/17270074000
Use it
Look up 17270-0740 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/17270-0740 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 17270-0740. 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.