Moxifloxacin PF
- Product NDC
- 71384-509
- 11-digit product format
- 713840509
- Labeler code
- 71384
- Product ID
- 71384-509_9ff912f9-a10e-cc5d-e053-2a95a90af150
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Moxifloxacin PF
- Dosage form
- INJECTION, SOLUTION
- Route
- OPHTHALMIC
- Labeler
- Imprimis NJOF, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-02-10
- 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
- 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 |
|---|
| 71384-509-01 | Moxifloxacin PF | 1 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 1 | | 10 |
| 71384-509-01 | Moxifloxacin PF | 20 in 1 BOX | INJECTION, SOLUTION | 20 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71384-509 | MOXIFLOXACIN PF INJECTION, SOLUTION [IMPRIMIS NJOF, LLC] | 10 | Legacy NDC, 2 package rows | 20200304_62fde226-6140-2364-e053-2a91aa0a68bb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71384-509-01 | 71384050901 | 20 VIAL, SINGLE-DOSE in 1 BOX (71384-509-01) > 1 mL in 1 VIAL, SINGLE-DOSE | 2020-02-10 | 0000-00-00 | No | No | Current |