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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53002-1550-12020-12-16C16284748780-19d75b9cf-ec00-f424-e053-dadaa90a57ce07b67416-139f-4e24-aab9-16285c9522ec
53002-1550-12020-01-31C16284748780-19d75b9cf-ec00-f424-e053-dadaa90a57ce07b67416-139f-4e24-aab9-16285c9522ec