PROAIR

Product NDC
49999-908
11-digit product format
499990908
Labeler code
49999
Product ID
49999-908_e1e27632-8721-4305-baaf-c7c2d59d4ab2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
albuterol sulfate
Dosage form
AEROSOL, METERED
Route
RESPIRATORY (INHALATION)
Labeler
Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Application
NDA021457
Marketing category
NDA
Marketing start
2012-03-21
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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49999-908-85GM - Gram49999-9088cad0cdf-5381-4721-af62-9bf88673d57112012-07-24