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
- 87063-031_430d292d-dcb0-a30d-e063-6294a90ae859
- Product NDC
- 87063-031
- Form
- SOLUTION
- Composition / generic term
- Albuterol Sulfate
- Labeler
- ASCLEMED USA INC.
- 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
- 30 POUCH in 1 CARTON (87063-031-01) / 1 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSE · 87063-031-01
- 1 POUCH in 1 CARTON (87063-031-25) / 25 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSE · 87063-031-25
- 1 POUCH in 1 CARTON (87063-031-30) / 30 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSE · 87063-031-30
- 2 POUCH in 1 CARTON (87063-031-60) / 30 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSE · 87063-031-60
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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