United States · FDA National Drug Code directory
CROMOLYN SODIUM
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
- 42571-132_22ffea9c-cd39-22dd-e063-6394a90aae4b
- Product NDC
- 42571-132
- Form
- SOLUTION, CONCENTRATE
- Composition / generic term
- Cromolyn sodium
- Labeler
- Micro Labs Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20130504
- Source listing expiry
- 20261231
Source-listed ingredients
- CROMOLYN SODIUM — 100 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 96 CARTON in 1 CARTON (42571-132-52) / 1 TRAY in 1 CARTON / 8 AMPULE in 1 TRAY / 5 mL in 1 AMPULE (42571-132-21) · 42571-132-52
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 →