Ciprofloxacin
- Product NDC
- 82868-070
- 11-digit product format
- 828680070
- Labeler code
- 82868
- Product ID
- 82868-070_476ba1ad-f80f-8ff0-e063-6294a90a11f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA077859
- Marketing category
- ANDA
- Marketing start
- 2025-01-21
- Marketing end
- 2027-01-31
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 250 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 | 250 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4BA73M5E37 |
| Rxcui | 197511 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82868-070-14 | Ciprofloxacin | 14 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 14 | | 3 |
| 82868-070-20 | Ciprofloxacin | 20 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 20 | | 3 |
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 |
|---|
| 82868-070-14 | 82868007014 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-070-14) | 2025-02-10 | 2027-01-31 | No | No | Historical |
| 82868-070-20 | 82868007020 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-070-20) | 2025-01-21 | 2027-01-31 | No | No | Historical |