NDC 69238-1345 – Albuterol

Albuterol Sulfate 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC69238-1345

Product details

Brand name
Albuterol
Generic name
Albuterol
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208804
Marketed since
May 24, 2018
Listing expires
December 31, 2027
Pharmacologic class
beta2-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Albuterol →

Package NDC codes (2)

Package NDCDescriptionSince
69238-1345-1100 TABLET in 1 BOTTLE (69238-1345-1)May 24, 2018
69238-1345-5500 TABLET in 1 BOTTLE (69238-1345-5)May 24, 2018

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