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
- 50742-392_250b033d-3ed5-c0d1-e063-6394a90a93c9
- Product NDC
- 50742-392
- Form
- SOLUTION
- Composition / generic term
- Albuterol Sulfate
- Labeler
- Ingenus Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241101
- Source listing expiry
- 20261231
Source-listed ingredients
- ALBUTEROL SULFATE — .63 mg/3mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 POUCH in 1 CARTON (50742-392-25) / 5 VIAL in 1 POUCH (50742-392-05) / 3 mL in 1 VIAL · 50742-392-25
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 →