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
- 71205-641_4263a4e9-a9d9-40da-ad2c-c75c82976319
- Product NDC
- 71205-641
- Form
- SOLUTION
- Composition / generic term
- albuterol sulfate
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210611
- Source listing expiry
- 20261231
Source-listed ingredients
- ALBUTEROL SULFATE — .83 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 POUCH in 1 CARTON (71205-641-25) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL · 71205-641-25
- 6 POUCH in 1 CARTON (71205-641-30) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL · 71205-641-30
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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