NDC 68084-949 – Albuterol Sulfate

Albuterol Sulfate 2 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68084-949

Product details

Brand name
Albuterol Sulfate
Generic name
Albuterol Sulfate
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA072637
Marketed since
September 22, 2015
Listing expires
December 31, 2026
Pharmacologic class
beta2-Adrenergic Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
68084-949-2530 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-949-25) / 1 TABLET in 1 BLISTER PACK (68084-949-95)Sep 22, 2015

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