Moxifloxacin
- Product NDC
- 50090-5279
- 11-digit product format
- 500905279
- Labeler code
- 50090
- Product ID
- 50090-5279_b659a45b-f713-41e4-a167-f286dd8324a9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Moxifloxacin
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- A-S Medication Solutions
- Application
- ANDA202916
- Marketing category
- ANDA
- Marketing start
- 2017-11-09
- 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
- 2022-12-31
- 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 |
|---|
| 50090-5279-0 | Moxifloxacin | 3 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 3 | | 1 |
| 50090-5279-0 | Moxifloxacin | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5279 | MOXIFLOXACIN SOLUTION/ DROPS [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 2 package rows | 20210116_ccc845e1-0a90-4c74-8659-4d798d8cf752.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5279-0 | 50090527900 | 1 BOTTLE, DROPPER in 1 CARTON (50090-5279-0) > 3 mL in 1 BOTTLE, DROPPER | 2020-10-21 | 0000-00-00 | No | No | Current |