PREDNISOLONE SODIUM PHOSPHATE
- Product NDC
- 13985-025
- 11-digit product format
- 139850025
- Labeler code
- 13985
- Product ID
- 13985-025_dbcab023-8a71-4c66-ac6b-b98b20a493f9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PREDNISOLONE SODIUM PHOSPHATE
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- MWI/VetOne
- Application
- ANDA040070
- Marketing category
- ANDA
- Marketing start
- 1994-07-29
- Marketing end
- 0000-00-00
- Substance
- PREDNISOLONE SODIUM PHOSPHATE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#