United States · FDA National Drug Code directory
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
- 50090-6560_9e4a9dac-8e00-4b2d-b3a1-2c9826e32e66
- Product NDC
- 50090-6560
- Form
- SOLUTION
- Composition / generic term
- Albuterol Sulfate
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19970917
- Source listing expiry
- 20261231
Source-listed ingredients
- ALBUTEROL SULFATE — 2.5 mg/3mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 POUCH in 1 CARTON (50090-6560-0) / 3 mL in 1 POUCH · 50090-6560-0
- 75 POUCH in 1 CARTON (50090-6560-1) / 3 mL in 1 POUCH · 50090-6560-1
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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