Ciprofloxacin
- Product NDC
- 72789-520
- 11-digit product format
- 727890520
- Labeler code
- 72789
- Product ID
- 72789-520_3c54f52e-9a55-3cd7-e063-6294a90a5bad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA077859
- Marketing category
- ANDA
- Marketing start
- 2024-02-09
- Marketing end
- 2028-02-29
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ciprofloxacin
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CIPROFLOXACIN HYDROCHLORIDE | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4BA73M5E37 |
| Rxcui | 309309 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72789-520-06 | Ciprofloxacin | 6 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 6 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72789-520-06 | 72789052006 | 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-520-06) | 2025-08-14 | 2028-02-29 | No | No | Historical |