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
- 50090-5735_1e119641-c50c-48a6-948c-b131a95908d4
- Product NDC
- 50090-5735
- Form
- INHALANT
- Composition / generic term
- albuterol sulfate
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200408
- Source listing expiry
- 20261231
Source-listed ingredients
- ALBUTEROL SULFATE — 90 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 96 CANISTER in 1 CASE (50090-5735-1) / 200 INHALANT in 1 CANISTER · 50090-5735-1
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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