Gati-Dex
- Product NDC
- 71384-506
- 11-digit product format
- 713840506
- Labeler code
- 71384
- Product ID
- 71384-506_638a1f49-53e8-7a69-e053-2991aa0a82bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gatifloxacin-Dexamethasone Phosphate
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Imprimis NJOF, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2018-01-05
- Marketing end
- 0000-00-00
- Substance
- DEXAMETHASONE SODIUM PHOSPHATE; GATIFLOXACIN
- Active strength
- 1 mg/mL; mg/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#