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
- 0487-9901_30dbae21-c906-0624-e063-6394a90a299c
- Product NDC
- 0487-9901
- Form
- SOLUTION
- Composition / generic term
- Albuterol Sulfate
- Labeler
- Nephron Pharmaceuticals Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20010626
- Source listing expiry
- 20261231
Source-listed ingredients
- ALBUTEROL SULFATE — 2.5 mg/.5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 BAG in 1 BOX (0487-9901-02) / 1 POUCH in 1 BAG / 1 VIAL, SINGLE-DOSE in 1 POUCH / .5 mL in 1 VIAL, SINGLE-DOSE · 0487-9901-02
- 30 POUCH in 1 CARTON (0487-9901-30) / 1 VIAL, SINGLE-DOSE in 1 POUCH / .5 mL in 1 VIAL, SINGLE-DOSE · 0487-9901-30
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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