Besivance
- Product NDC
- 82260-466
- 11-digit product format
- 822600466
- Labeler code
- 82260
- Product ID
- 82260-466_483360bc-332c-6ccd-e063-6394a90a0b25
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Besifloxacin
- Dosage form
- SUSPENSION
- Route
- OPHTHALMIC
- Labeler
- Bausch & Lomb Americas Inc.
- Application
- NDA022308
- Marketing category
- NDA
- Marketing start
- 2026-01-09
- Substance
- BESIFLOXACIN
- Active strength
- 6 mg/mL
- Pharmacologic classes
- Quinolone Antimicrobial [EPC], Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Besivance
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BESIFLOXACIN | 6 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | BFE2NBZ7NX |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82260-466-05 | Besivance | 1 in 1 CARTON | SUSPENSION | 1 | | 1 |
| 82260-466-05 | Besivance | 5 mL in 1 BOTTLE, DROPPER | SUSPENSION | 5 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 82260-466-05 | 82260046605 | 1 BOTTLE, DROPPER in 1 CARTON (82260-466-05) / 5 mL in 1 BOTTLE, DROPPER | 2026-01-09 | No | No | Current |