Dex-Moxi
- Product NDC
- 71384-512
- 11-digit product format
- 713840512
- Labeler code
- 71384
- Product ID
- 71384-512_9e3f348b-d46a-6ff1-e053-2995a90a7c1c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone Phosphate - Moxifloxacin
- Dosage form
- INJECTION, SOLUTION
- Route
- OPHTHALMIC
- Labeler
- Imprimis NJOF, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2018-01-05
- Marketing end
- 0000-00-00
- Substance
- DEXAMETHASONE SODIUM PHOSPHATE; MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE
- Active strength
- 1 mg/mL; mg/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],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 |
|---|
| 71384-512-01 | Dex-Moxi | 1 mL in 1 VIAL, SINGLE-USE | INJECTION, SOLUTION | 1 | | 4 |
| 71384-512-01 | Dex-Moxi | 20 in 1 BOX | INJECTION, SOLUTION | 20 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71384-512 | DEX-MOXI (DEXAMETHASONE PHOSPHATE - MOXIFLOXACIN) INJECTION, SOLUTION [IMPRIMIS NJOF, LLC] | 4 | Legacy NDC, 2 package rows | 20200211_62ff1da3-7998-676a-e053-2991aa0a4a9f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71384-512-01 | 71384051201 | 20 VIAL, SINGLE-USE in 1 BOX (71384-512-01) > 1 mL in 1 VIAL, SINGLE-USE | 2018-01-05 | 0000-00-00 | No | No | Current |