Albuterol Sulate HFA
NDC 70518-2072, albuterol sulfate, aerosol, metered, from REMEDYREPACK INC..
- Product NDC
- 70518-2072
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA020983
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2072 \ -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 |
|---|---|---|
| 70518-2072-0 | 70518207200 | 1 INHALER in 1 CARTON (70518-2072-0) / 200 AEROSOL, METERED in 1 INHALER |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/77d34a3c-ccc6-420a-ad31-a1af55f7de76
Use it
Look up 70518-2072 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2072 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-2072. 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.