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
- 0054-0742_07a1b9ad-58cb-4c21-b8df-6854da990f85
- Product NDC
- 0054-0742
- Form
- AEROSOL, METERED
- Composition / generic term
- Albuterol Sulfate
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211130
- Source listing expiry
- 20261231
Source-listed ingredients
- ALBUTEROL SULFATE — 90 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 CANISTER in 1 CARTON (0054-0742-87) / 200 AEROSOL, METERED in 1 CANISTER · 0054-0742-87
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 →