NDC 62135-672 – Albuterol Sulfate

Albuterol Sulfate 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC62135-672

Product details

Brand name
Albuterol Sulfate
Generic name
Albuterol Sulfate
Labeler
Chartwell RX, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA072151
Marketed since
December 5, 1989
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
62135-672-9090 TABLET in 1 BOTTLE (62135-672-90)Jun 14, 2023

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