United States · FDA National Drug Code directory
Ipratropium Bromide and Albuterol Sulfate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0487-0201_32473735-b131-709c-e063-6294a90afde8
- Product NDC
- 0487-0201
- Form
- SOLUTION
- Composition / generic term
- Ipratropium Bromide and Albuterol Sulfate
- Labeler
- Nephron Pharmaceuticals Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20071231
- Source listing expiry
- 20261231
Source-listed ingredients
- IPRATROPIUM BROMIDE — .5 mg/3mL
- ALBUTEROL SULFATE — 3 mg/3mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 POUCH in 1 CARTON (0487-0201-01) / 1 VIAL, SINGLE-USE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-USE · 0487-0201-01
- 30 POUCH in 1 CARTON (0487-0201-02) / 1 VIAL, SINGLE-USE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-USE · 0487-0201-02
- 6 POUCH in 1 CARTON (0487-0201-03) / 5 VIAL, SINGLE-USE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-USE · 0487-0201-03
- 12 POUCH in 1 CARTON (0487-0201-60) / 5 VIAL, SINGLE-USE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-USE · 0487-0201-60
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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