Ciprofloxacin
- Product NDC
- 71205-649
- 11-digit product format
- 712050649
- Labeler code
- 71205
- Product ID
- 71205-649_00f44d29-72b5-47a6-a26a-eb1f1c430917
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA077859
- Marketing category
- ANDA
- Marketing start
- 2007-04-26
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 4BA73M5E37 | CIPROFLOXACIN HYDROCHLORIDE | 86393-32-0 | CIPROFLOXACIN HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-649-06 | 71205064906 | 6 TABLET, FILM COATED in 1 BOTTLE (71205-649-06) | 2022-03-28 | No | No | Historical |
| 71205-649-07 | 71205064907 | 7 TABLET, FILM COATED in 1 BOTTLE (71205-649-07) | 2024-06-26 | No | No | Historical |
| 71205-649-10 | 71205064910 | 10 TABLET, FILM COATED in 1 BOTTLE (71205-649-10) | 2022-03-28 | No | No | Historical |
| 71205-649-14 | 71205064914 | 14 TABLET, FILM COATED in 1 BOTTLE (71205-649-14) | 2022-03-28 | No | No | Historical |
| 71205-649-20 | 71205064920 | 20 TABLET, FILM COATED in 1 BOTTLE (71205-649-20) | 2022-03-28 | No | No | Historical |
| 71205-649-30 | 71205064930 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-649-30) | 2022-03-28 | No | No | Historical |
| 71205-649-60 | 71205064960 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-649-60) | 2022-03-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ciprofloxacin | Proficient Rx LP | 2024-06-01 | HUMAN PRESCRIPTION DRUG LABEL | 4 |