albuterol sulfate

Product NDC
63629-2638
11-digit product format
636292638
Labeler code
63629
Product ID
63629-2638_322f5d1e-0c44-4e67-8c7c-af2d8c8ffa57
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
albuterol sulfate
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA072637
Marketing category
ANDA
Marketing start
1989-12-05
Marketing end
0000-00-00
Substance
ALBUTEROL SULFATE
Active strength
2 mg/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#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-2638-1EA - Each63629-2638c26ecb66-8ffc-4e97-b4e9-6998aa3d83a612012-07-24
63629-2638-2EA - Each63629-263851a9a1a6-4c0e-482a-87db-c2e88ad3f12312012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-2638-16362926380120 TABLET in 1 BOTTLE (63629-2638-1) 20 tablet2010-06-020000-00-00NoNoCurrent
63629-2638-26362926380230 TABLET in 1 BOTTLE (63629-2638-2) 30 tablet2010-06-020000-00-00NoNoCurrent
63629-2638-36362926380360 TABLET in 1 BOTTLE (63629-2638-3) 60 tablet2005-04-110000-00-00NoNoCurrent
63629-2638-46362926380490 TABLET in 1 BOTTLE (63629-2638-4) 90 tablet2005-04-110000-00-00NoNoCurrent