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
- 81665-104_fd09b0f1-907c-4d4d-a693-9756efd60f20
- Product NDC
- 81665-104
- Form
- SOLUTION, CONCENTRATE
- Composition / generic term
- CROMOLYN SODIUM
- Labeler
- Omnivium Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240831
- Source listing expiry
- 20271231
Source-listed ingredients
- CROMOLYN SODIUM — 100 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 12 POUCH in 1 CARTON (81665-104-96) / 8 AMPULE in 1 POUCH / 5 mL in 1 AMPULE · 81665-104-96
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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