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
- 63629-2611_3352d236-01ed-a102-e063-6294a90a2a8d
- Product NDC
- 63629-2611
- Form
- TABLET
- Composition / generic term
- albuterol
- Labeler
- Bryant Ranch Prepack
- 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
- 20 TABLET in 1 BOTTLE (63629-2611-1) · 63629-2611-1
- 30 TABLET in 1 BOTTLE (63629-2611-2) · 63629-2611-2
- 60 TABLET in 1 BOTTLE (63629-2611-3) · 63629-2611-3
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 →