Fluorescein Sodium and Benoxinate Hydrochloride
- Product NDC
- 24208-732
- 11-digit product format
- 242080732
- Labeler code
- 24208
- Product ID
- 24208-732_ca1981e3-3b68-46f9-95b5-db9dc481eaa5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluorescein Sodium and Benoxinate Hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Bausch & Lomb Incorporated
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1995-01-01
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record