Cromolyn Sodium
- Product NDC
- 50090-3125
- 11-digit product format
- 500903125
- Labeler code
- 50090
- Product ID
- 50090-3125_fde851bc-b138-4062-8978-cebe49455c2e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cromolyn sodium
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- A-S Medication Solutions
- Application
- ANDA074443
- Marketing category
- ANDA
- Marketing start
- 1995-01-30
- Marketing end
- 0000-00-00
- Substance
- CROMOLYN SODIUM
- Active strength
- 40 mg/mL
- Pharmacologic classes
- Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record