Ciprofloxacin
- Product NDC
- 60760-690
- 11-digit product format
- 607600690
- Labeler code
- 60760
- Product ID
- 60760-690_348e9276-54df-fa85-e063-6394a90a5d26
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofolxacin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA208921
- Marketing category
- ANDA
- Marketing start
- 2023-10-01
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 250 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
Additional Listing Data
- Finished product
- Yes
- Brand name base
- Ciprofloxacin
- Listing expiration
- 2026-12-31
Active Ingredients
| Ingredient | Strength |
|---|
| CIPROFLOXACIN HYDROCHLORIDE | 250 mg/1 |
Harmonized Identifiers
| Field | Values |
|---|
| Unii | 4BA73M5E37 |
| Rxcui | 197511 |
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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60760-690-10 | 60760069010 | 10 TABLET in 1 BOTTLE, PLASTIC (60760-690-10) | 10 tablet | 2025-05-07 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ciprofloxacin | ST. MARY'S MEDICAL PARK PHARMACY | 2025-05-07 | HUMAN PRESCRIPTION DRUG LABEL | 1 |