NDC 0487-0201 – Ipratropium Bromide and Albuterol Sulfate

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

Human Prescription Drug 2 recalls

Product NDC0487-0201

Product details

Brand name
Ipratropium Bromide and Albuterol Sulfate
Generic name
Ipratropium Bromide and Albuterol Sulfate
Labeler
Nephron Pharmaceuticals Corporation
Dosage form
Solution
Route
Respiratory (inhalation)
Marketing category
ANDA · ANDA076749
Marketed since
December 31, 2007
Listing expires
December 31, 2026
Pharmacologic class
Anticholinergic; beta2-Adrenergic Agonist

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
0487-0201-0130 POUCH in 1 CARTON (0487-0201-01) / 1 VIAL, SINGLE-USE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-USEDec 31, 2007
0487-0201-0230 POUCH in 1 CARTON (0487-0201-02) / 1 VIAL, SINGLE-USE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-USEDec 31, 2007
0487-0201-036 POUCH in 1 CARTON (0487-0201-03) / 5 VIAL, SINGLE-USE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-USEDec 31, 2007
0487-0201-6012 POUCH in 1 CARTON (0487-0201-60) / 5 VIAL, SINGLE-USE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-USEDec 31, 2007

Recalls mentioning this NDC

Other Ipratropium Bromide and Albuterol Sulfate products