Ofloxacin
- Product NDC
- 71205-682
- 11-digit product format
- 712050682
- Labeler code
- 71205
- Product ID
- 71205-682_e517e70f-da42-4421-98cc-5a31e84f1d45
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ofloxaxin
- Dosage form
- SOLUTION/ DROPS
- Route
- AURICULAR (OTIC)
- Labeler
- Proficient Rx LP
- Application
- ANDA076616
- Marketing category
- ANDA
- Marketing start
- 2008-03-17
- Marketing end
- 0000-00-00
- Substance
- OFLOXACIN
- Active strength
- 3 mg/mL
- Pharmacologic classes
- Quinolone Antimicrobial [EPC], Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-682 | OFLOXACIN (OFLOXAXIN) SOLUTION/ DROPS [PROFICIENT RX LP] | 1 | Legacy NDC | 20220811_e517e70f-da42-4421-98cc-5a31e84f1d45.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-682-05 | 71205068205 | 1 BOTTLE in 1 CARTON (71205-682-05) > 5 mL in 1 BOTTLE | 1 bottle | 2022-08-09 | 0000-00-00 | No | No | Current |