PROAIR
- Product NDC
- 53002-1550
- 11-digit product format
- 530021550
- Labeler code
- 53002
- Product ID
- 53002-1550_cf8faecc-0740-4a6f-aa44-76c4886d5d23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- NDA021457
- Marketing category
- NDA
- Marketing start
- 2012-12-03
- Marketing end
- 0000-00-00
- Substance
- ALBUTEROL SULFATE
- Active strength
- 90 ug/1
- Pharmacologic classes
- Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#