NDC product
Albuterol Sulfate
NDC 17270-0740 · Armstrong Pharmaceuticals, Inc.
Key facts
| Product NDC | 17270-0740 |
|---|---|
| Proprietary name | Albuterol Sulfate |
| Nonproprietary name | Albuterol Sulfate |
| Substances | ALBUTEROL SULFATE |
| Dosage form | INHALANT |
| Route | RESPIRATORY (INHALATION) |
| Labeler | Armstrong Pharmaceuticals, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA212447 |
| Pharmacologic classes | Adrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC] |
| Marketing start | Aug 6, 2024 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: