NDC 69097-173 – Ipratropium Bromide and Albuterol Sulfate

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

Human Prescription Drug 1 recall

Product NDC69097-173

Product details

Brand name
Ipratropium Bromide and Albuterol Sulfate
Generic name
Ipratropium Bromide and Albuterol Sulfate
Labeler
Cipla USA Inc.
Dosage form
Solution
Route
Respiratory (inhalation)
Marketing category
ANDA · ANDA077559
Marketed since
December 31, 2007
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
69097-173-536 POUCH in 1 CARTON (69097-173-53) / 5 VIAL in 1 POUCH / 3 mL in 1 VIALDec 31, 2007
69097-173-6412 POUCH in 1 CARTON (69097-173-64) / 5 VIAL in 1 POUCH / 3 mL in 1 VIALDec 31, 2007

Recalls mentioning this NDC

Other Ipratropium Bromide and Albuterol Sulfate products