United States · FDA National Drug Code directory
Isoproterenol Hydrochloride
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
- 42571-294_ed7a8636-e10f-71c6-e053-2995a90a728b
- Product NDC
- 42571-294
- Form
- INJECTION
- Composition / generic term
- Isoproterenol Hydrochloride
- Labeler
- Micro Labs Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210501
- Source listing expiry
- 20261231
Source-listed ingredients
- ISOPROTERENOL HYDROCHLORIDE — .2 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 CARTON in 1 CARTON (42571-294-79) / 5 AMPULE in 1 CARTON (42571-294-78) / 1 mL in 1 AMPULE · 42571-294-79
Source and coverage
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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.
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