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
- 51662-1499_2b387337-c48e-7eb1-e063-6294a90a9cba
- Product NDC
- 51662-1499
- Form
- SOLUTION
- Composition / generic term
- ALBUTEROL SULFATE
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200129
- Source listing expiry
- 20261231
Source-listed ingredients
- ALBUTEROL SULFATE — 2.5 mg/3mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 VIAL, SINGLE-DOSE in 1 POUCH (51662-1499-1) / 3 mL in 1 VIAL, SINGLE-DOSE · 51662-1499-1
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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