NDC 0487-9801 – Ipratropium Bromide

Ipratropium Bromide .5 mg/2.5mL · Solution · Respiratory (inhalation)

Human Prescription Drug 1 recall

Product NDC0487-9801

Product details

Brand name
Ipratropium Bromide
Generic name
Ipratropium Bromide
Labeler
Nephron Pharmaceuticals Corporation
Dosage form
Solution
Route
Respiratory (inhalation)
Marketing category
ANDA · ANDA075562
Marketed since
September 27, 2001
Listing expires
December 31, 2026
Pharmacologic class
Anticholinergic

Active ingredients

Uses, dosage, side effects and warnings for Ipratropium bromide →

Package NDC codes (5)

Package NDCDescriptionSince
0487-9801-0130 POUCH in 1 CARTON (0487-9801-01) / 1 VIAL, SINGLE-DOSE in 1 POUCH / 2.5 mL in 1 VIAL, SINGLE-DOSESep 27, 2001
0487-9801-0230 BAG in 1 BOX (0487-9801-02) / 1 POUCH in 1 BAG / 1 VIAL, SINGLE-DOSE in 1 POUCH / 2.5 mL in 1 VIAL, SINGLE-DOSESep 27, 2001
0487-9801-251 POUCH in 1 CARTON (0487-9801-25) / 25 VIAL, SINGLE-DOSE in 1 POUCH / 2.5 mL in 1 VIAL, SINGLE-DOSESep 27, 2001
0487-9801-301 POUCH in 1 CARTON (0487-9801-30) / 30 VIAL, SINGLE-DOSE in 1 POUCH / 2.5 mL in 1 VIAL, SINGLE-DOSESep 27, 2001
0487-9801-602 POUCH in 1 CARTON (0487-9801-60) / 30 VIAL, SINGLE-DOSE in 1 POUCH / 2.5 mL in 1 VIAL, SINGLE-DOSESep 27, 2001

Recalls mentioning this NDC

Other Ipratropium bromide products