Ciprofloxacin
- Product NDC
- 71205-636
- 11-digit product format
- 712050636
- Labeler code
- 71205
- Product ID
- 71205-636_e72981fd-0d15-473b-8e3d-ee84e3d71c03
- 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
- 250 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC], Quinolones [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 |
|---|
| 71205-636-06 | 71205063606 | 6 TABLET, FILM COATED in 1 BOTTLE (71205-636-06) | 2022-02-02 | No | No | Historical |
| 71205-636-10 | 71205063610 | 10 TABLET, FILM COATED in 1 BOTTLE (71205-636-10) | 2022-02-02 | No | No | Historical |
| 71205-636-14 | 71205063614 | 14 TABLET, FILM COATED in 1 BOTTLE (71205-636-14) | 2022-02-03 | No | No | Historical |
| 71205-636-20 | 71205063620 | 20 TABLET, FILM COATED in 1 BOTTLE (71205-636-20) | 2022-02-02 | No | No | Historical |
| 71205-636-30 | 71205063630 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-636-30) | 2022-02-02 | No | No | Historical |
| 71205-636-60 | 71205063660 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-636-60) | 2022-02-02 | No | No | Historical |
| 71205-636-90 | 71205063690 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-636-90) | 2022-02-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ciprofloxacin | Proficient Rx LP | 2022-07-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |