FLUOROMETHOLONE
- Product NDC
- 70518-1929
- 11-digit product format
- 705181929
- Labeler code
- 70518
- Product ID
- 70518-1929_8312d106-8da0-d782-e053-2a91aa0a47d6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fluorometholone
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- REMEDYREPACK INC.
- Application
- NDA016851
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-03-01
- Marketing end
- 0000-00-00
- Substance
- FLUOROMETHOLONE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record