Albuterol Sulfate

Product NDC
0781-7155
11-digit product format
007817155
Labeler code
0781
Product ID
0781-7155_5fb1a243-8c4d-d584-e053-2991aa0ae1cb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Albuterol Sulfate
Dosage form
SOLUTION
Route
RESPIRATORY (INHALATION)
Labeler
Sandoz Inc.
Application
ANDA077839
Marketing category
ANDA
Marketing start
2011-08-17
Marketing end
0000-00-00
Substance
ALBUTEROL SULFATE
Active strength
3 mg/3mL
Pharmacologic classes
Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-7155-29ML - Milliliter0781-7155599eecc6-f244-4998-bd46-e5065265611812012-07-24
0781-7155-64ML - Milliliter0781-7155f904b95f-22f0-4f56-a549-1ff101015fc612012-07-24
0781-7155-86ML - Milliliter0781-71552df9f755-0887-438b-a3ca-73b8f568ecba12012-07-24