Ciprofloxacin
- Product NDC
- 70934-790
- 11-digit product format
- 709340790
- Labeler code
- 70934
- Product ID
- 70934-790_b116c473-1e30-1b8f-e053-2a95a90a34f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA076558
- Marketing category
- ANDA
- Marketing start
- 2020-09-02
- Marketing end
- 0000-00-00
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 4BA73M5E37 | CIPROFLOXACIN HYDROCHLORIDE | 86393-32-0 | CIPROFLOXACIN HYDROCHLORIDE |
| 5E8K9I0O4U | CIPROFLOXACIN | 85721-33-1 | Ciprofloxacin |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-790-06 | 70934079006 | 6 TABLET, FILM COATED in 1 BOTTLE, GLASS (70934-790-06) | 2020-09-02 | 0000-00-00 | No | No | Current |
| 70934-790-14 | 70934079014 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-790-14) | 2020-09-08 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ciprofloxacin | Denton Pharma, Inc. dba Northwind Pharmaceuticals | 2020-10-07 | HUMAN PRESCRIPTION DRUG LABEL | 1 |