United States · FDA National Drug Code directory
Albuterol Sulfate HFA
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
- 66993-019_70817038-c7c0-4978-b5a2-0f6a0267ae33
- Product NDC
- 66993-019
- Form
- AEROSOL, METERED
- Composition / generic term
- albuterol sulfate
- Labeler
- Prasco Laboratories
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20190115
- Source listing expiry
- 20271231
Source-listed ingredients
- ALBUTEROL SULFATE — 90 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 INHALER in 1 CARTON (66993-019-68) / 200 AEROSOL, METERED in 1 INHALER · 66993-019-68
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 →