United States · FDA National Drug Code directory
Albuterol
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
- 64980-443_f3d2f709-6e2e-4c25-8069-52661dc76e2d
- Product NDC
- 64980-443
- Form
- TABLET
- Composition / generic term
- albuterol
- Labeler
- Rising Pharma Holdings, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180629
- Source listing expiry
- 20261231
Source-listed ingredients
- ALBUTEROL SULFATE — 4 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (64980-443-01) · 64980-443-01
- 500 TABLET in 1 BOTTLE (64980-443-50) · 64980-443-50
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 →