ALTAFLUOR
- Product NDC
- 59390-206
- 11-digit product format
- 593900206
- Labeler code
- 59390
- Product ID
- 59390-206_3f415ffe-f95c-418b-9ee3-a1e34670a4e5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluorescein Sodium and Benoxinate Hydrochloride
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- Altaire Pharmaceuticals Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2000-06-21
- Marketing end
- 0000-00-00
- Substance
- BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM
- Active strength
- 4 mg/mL; mg/mL
- Pharmacologic classes
- Diagnostic Dye [EPC],Dyes [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record