United States · FDA National Drug Code directory
ISOPROTERENOL
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
- 69097-521_6014b0c8-2851-4111-a4f7-6764be850176
- Product NDC
- 69097-521
- Form
- INJECTION, SOLUTION
- Composition / generic term
- isoproterenol hydrochloride
- Labeler
- Cipla USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180626
- Source listing expiry
- 20261231
Source-listed ingredients
- ISOPROTERENOL HYDROCHLORIDE — .2 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 AMPULE in 1 CARTON (69097-521-31) / 1 mL in 1 AMPULE · 69097-521-31
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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