Cromolyn Sodium
- Product NDC
- 68071-3231
- 11-digit product format
- 680713231
- Labeler code
- 68071
- Product ID
- 68071-3231_51ca74fe-3364-65dc-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cromolyn sodium
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- NuCare Pharmaceuticals, Inc.
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record