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
- 68788-8490_378bf83b-f080-45f8-a53a-0dc2f32f4cac
- Product NDC
- 68788-8490
- Form
- SOLUTION/ DROPS
- Composition / generic term
- Cromolyn Sodium
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230721
- Source listing expiry
- 20271231
Source-listed ingredients
- CROMOLYN SODIUM — 40 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 mL in 1 BOTTLE, PLASTIC (68788-8490-1) · 68788-8490-1
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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