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
- 69097-142_135ef57d-f447-45c6-ad56-e4f772dc98ee
- Product NDC
- 69097-142
- Form
- INHALANT
- Composition / generic term
- albuterol sulfate
- Labeler
- Cipla USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200408
- Source listing expiry
- 20271231
Source-listed ingredients
- ALBUTEROL SULFATE — 90 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 CANISTER in 1 CARTON (69097-142-60) / 200 INHALANT in 1 CANISTER · 69097-142-60
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 →