NDC 70771-1512 – Albuterol

Albuterol Sulfate 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70771-1512

Product details

Brand name
Albuterol
Generic name
Albuterol
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208884
Marketed since
October 23, 2020
Listing expires
December 31, 2026
Pharmacologic class
beta2-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Albuterol →

Package NDC codes (2)

Package NDCDescriptionSince
70771-1512-1100 TABLET in 1 BOTTLE (70771-1512-1)Oct 23, 2020
70771-1512-5500 TABLET in 1 BOTTLE (70771-1512-5)Oct 23, 2020

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