NDC 53489-176 – albuterol sulfate

Albuterol Sulfate 2 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC53489-176

Product details

Brand name
albuterol sulfate
Generic name
albuterol sulfate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA072637
Marketed since
December 5, 1989
Listing expires
December 31, 2027
Pharmacologic class
beta2-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Albuterol Sulfate →

Package NDC codes (5)

Package NDCDescriptionSince
53489-176-01100 TABLET in 1 BOTTLE (53489-176-01)Dec 5, 1989
53489-176-0250 TABLET in 1 BOTTLE (53489-176-02)Dec 5, 1989
53489-176-03250 TABLET in 1 BOTTLE (53489-176-03)Dec 5, 1989
53489-176-05500 TABLET in 1 BOTTLE (53489-176-05)Dec 5, 1989
53489-176-101000 TABLET in 1 BOTTLE (53489-176-10)Dec 5, 1989

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