United States · FDA National Drug Code directory
Ipratropium Bromide
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
- 47335-706_147b55d9-c9f9-4a22-814a-acf834a1864d
- Product NDC
- 47335-706
- Form
- SOLUTION
- Composition / generic term
- Ipratropium Bromide
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200204
- Source listing expiry
- 20261231
Source-listed ingredients
- IPRATROPIUM BROMIDE — .5 mg/2.5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 POUCH in 1 CARTON (47335-706-49) / 5 VIAL in 1 POUCH (47335-706-48) / 2.5 mL in 1 VIAL · 47335-706-49
- 6 POUCH in 1 CARTON (47335-706-52) / 5 VIAL in 1 POUCH / 2.5 mL in 1 VIAL · 47335-706-52
- 12 POUCH in 1 CARTON (47335-706-54) / 5 VIAL in 1 POUCH / 2.5 mL in 1 VIAL · 47335-706-54
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 →