United States · FDA National Drug Code directory
Ipratropium Bromide and 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
- 47335-756_c0e6d8e4-e189-480c-8a4c-f52dda4c6dc5
- Product NDC
- 47335-756
- Form
- SOLUTION
- Composition / generic term
- Ipratropium Bromide and Albuterol Sulfate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211115
- Source listing expiry
- 20271231
Source-listed ingredients
- IPRATROPIUM BROMIDE — .5 mg/3mL
- ALBUTEROL SULFATE — 2.5 mg/3mL
These values do not establish equivalence or a dose recommendation.
Packages
- 6 POUCH in 1 CARTON (47335-756-49) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL · 47335-756-49
- 12 POUCH in 1 CARTON (47335-756-52) / 5 VIAL in 1 POUCH / 3 mL in 1 VIAL · 47335-756-52
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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