Dex-Moxi PF
- Product NDC
- 70261-512
- 11-digit product format
- 702610512
- Labeler code
- 70261
- Product ID
- 70261-512_6bb78fd2-5d73-1b41-e053-2991aa0af497
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dexamethasone - 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
- 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
- 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 |
|---|
| 70261-512-01 | Dex-Moxi PF | 1 mL in 1 VIAL, SINGLE-USE | INJECTION, SOLUTION | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70261-512 | DEX-MOXI PF (DEXAMETHASONE - MOXIFLOXACIN PF) INJECTION, SOLUTION [IMPRIMISRX NJ] | 1 | Legacy NDC, 1 package rows | 20180509_6bb78fd2-5d72-1b41-e053-2991aa0af497.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 70261-512-01 | 70261051201 | 1 mL in 1 VIAL, SINGLE-USE | 1 ml | Historical |