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
- 64980-641_56c01144-7ba7-2f75-e063-6294a90a6e6f
- Product NDC
- 64980-641
- Form
- SOLUTION
- Composition / generic term
- Albuterol Sulfate
- Labeler
- Rising Pharma Holdings, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250314
- Source listing expiry
- 20271231
Source-listed ingredients
- ALBUTEROL SULFATE — 2.5 mg/3mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 POUCH in 1 CARTON (64980-641-02) / 25 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSE · 64980-641-02
- 1 POUCH in 1 CARTON (64980-641-03) / 30 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSE · 64980-641-03
- 2 POUCH in 1 CARTON (64980-641-06) / 30 VIAL, SINGLE-DOSE in 1 POUCH / 3 mL in 1 VIAL, SINGLE-DOSE · 64980-641-06
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 →