NDC 47335-756 – Ipratropium Bromide and Albuterol Sulfate

Ipratropium Bromide .5 mg/3mL; Albuterol Sulfate 2.5 mg/3mL · Solution · Respiratory (inhalation)

Human Prescription Drug

Product NDC47335-756

Product details

Brand name
Ipratropium Bromide and Albuterol Sulfate
Generic name
Ipratropium Bromide and Albuterol Sulfate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Solution
Route
Respiratory (inhalation)
Marketing category
ANDA · ANDA207875
Marketed since
November 15, 2021
Listing expires
December 31, 2027
Pharmacologic class
Anticholinergic; beta2-Adrenergic Agonist

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
47335-756-496 POUCH in 1 CARTON (47335-756-49) / 5 VIAL in 1 POUCH / 3 mL in 1 VIALNov 15, 2021
47335-756-5212 POUCH in 1 CARTON (47335-756-52) / 5 VIAL in 1 POUCH / 3 mL in 1 VIALNov 15, 2021

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