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
- 50090-1669_8fcfdb22-8586-4ad6-8ec9-ab0a9f09ab98
- Product NDC
- 50090-1669
- Form
- SOLUTION
- Composition / generic term
- Ipratropium Bromide and Albuterol Sulfate
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20071231
- Source listing expiry
- 20271231
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 VIAL, SINGLE-DOSE in 1 POUCH (50090-1669-0) / 3 mL in 1 VIAL, SINGLE-DOSE · 50090-1669-0
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →