Ciprofloxacin
- Product NDC
- 72789-125
- 11-digit product format
- 727890125
- Labeler code
- 72789
- Product ID
- 72789-125_2d675959-9721-1fd0-e063-6294a90aad29
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA076558
- Marketing category
- ANDA
- Marketing start
- 2004-06-09
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 750 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 table| Ingredient | Strength |
|---|
| CIPROFLOXACIN HYDROCHLORIDE | 750 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4BA73M5E37 |
| Rxcui | 197511, 197512 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72789-125-50 | Ciprofloxacin | 50 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 50 | | 27 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-125 | CIPROFLOXACIN TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.] | 27 | Current NDC, Legacy NDC, 1 package rows | 20250207_5723eaf9-8659-4730-b792-4e4c33690ccb.zip |
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 |
|---|
| 72789-125-50 | 72789012550 | 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-125-50) | 2020-10-07 | 0000-00-00 | No | No | Current |