Albuterol Sulfate 47335-0703-49

Package NDC

47335-0703-49

Manufacturer: Sun Pharmaceutical Industries, Inc.
Dosage Form: Solution
Route: Respiratory (inhalation)
Product Type: Human Prescription Drug
Marketing Start: June 11, 2021
Listing Expires: December 31, 2027
Application: ANDA207857

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Active Ingredients

Ingredient	Strength
Albuterol Sulfate	.83 mg/mL

Drug Class

Adrenergic beta2-Agonists [MoA]beta2-Adrenergic Agonist [EPC]

Selected Package

47335-0703-49Selected

5 POUCH in 1 CARTON (47335-703-49) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL

Other packages for this product(2)

47335-0703-52

6 POUCH in 1 CARTON (47335-703-52) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL

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47335-0703-54

12 POUCH in 1 CARTON (47335-703-54) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL

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