MOXIFLOXACIN
- Product NDC
- 72189-076
- 11-digit product format
- 721890076
- Labeler code
- 72189
- Product ID
- 72189-076_9ffa08ea-c456-80b7-e053-2a95a90a4bd6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MOXIFLOXACIN
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- DIRECT RX
- Application
- ANDA206242
- Marketing category
- ANDA
- Marketing start
- 2020-03-04
- Marketing end
- 0000-00-00
- Substance
- MOXIFLOXACIN HYDROCHLORIDE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-076-05 | MOXIFLOXACIN | 3 mL in 1 BOTTLE | SOLUTION/ DROPS | 3 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-076 | MOXIFLOXACIN SOLUTION/ DROPS [DIRECT RX] | 1 | Legacy NDC, 1 package rows | 20200305_9ffa08ea-c455-80b7-e053-2a95a90a4bd6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72189-076-05 | 72189007605 | 3 mL in 1 BOTTLE (72189-076-05) | 3 ml | 2020-03-04 | 0000-00-00 | No | No | Current |