Moxifloxacin
- Product NDC
- 72162-2107
- 11-digit product format
- 721622107
- Labeler code
- 72162
- Product ID
- 72162-2107_5e65bcf7-98de-4ec2-adf9-cbb8ec0bbe68
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- moxifloxacin
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090080
- Marketing category
- ANDA
- Marketing start
- 2017-07-01
- Substance
- MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Moxifloxacin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE | 5 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | B8956S8609 |
| Rxcui | 403818 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2107-2 | Moxifloxacin | 3 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 3 | | 101 |
| 72162-2107-2 | Moxifloxacin | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2107 | MOXIFLOXACIN SOLUTION/ DROPS [BRYANT RANCH PREPACK] | 101 | Current NDC, 2 package rows | 20241011_1cc031d7-0766-41c0-b5b3-35119c850e23.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2107-2 | 72162210702 | 1 BOTTLE, DROPPER in 1 CARTON (72162-2107-2) / 3 mL in 1 BOTTLE, DROPPER | 2017-07-01 | No | No | Current |