CIPROFLOXACIN
- Product NDC
- 72189-323
- 11-digit product format
- 721890323
- Labeler code
- 72189
- Product ID
- 72189-323_2c3d4146-03d9-30a9-e063-6294a90ad471
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- CIPROFLOXACIN
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Direct Rx
- Application
- ANDA208921
- Marketing category
- ANDA
- Marketing start
- 2022-02-21
- 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 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 |
|---|
| 72189-323-06 | CIPROFLOXACIN | 6 in 1 BOTTLE | TABLET, COATED | 6 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-323 | CIPROFLOXACIN TABLET, COATED [DIRECT RX] | 2 | Current NDC, Legacy NDC, 1 package rows | 20250122_d88a22f4-2f61-17f2-e053-2995a90acd14.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 |
|---|
| 72189-323-06 | 72189032306 | 6 TABLET, COATED in 1 BOTTLE (72189-323-06) | 2022-02-21 | 0000-00-00 | No | No | Current |