Moxifloxacin PF
- Product NDC
- 70261-511
- 11-digit product format
- 702610511
- Labeler code
- 70261
- Product ID
- 70261-511_6bb744c0-b613-2858-e053-2991aa0ae715
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Moxifloxacin PF
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAOCULAR
- Labeler
- ImprimisRx NJ
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2018-01-01
- Marketing end
- 0000-00-00
- Substance
- MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 70261-511-01 | Moxifloxacin PF | 1 mL in 1 VIAL, GLASS | INJECTION, SOLUTION | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70261-511 | MOXIFLOXACIN PF INJECTION, SOLUTION [IMPRIMISRX NJ] | 1 | Legacy NDC, 1 package rows | 20180509_6bb744c0-b612-2858-e053-2991aa0ae715.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 70261-511-01 | 70261051101 | 1 mL in 1 VIAL, GLASS | 1 ml | Historical |