ciprofloxacin
- Product NDC
- 45865-530
- 11-digit product format
- 458650530
- Labeler code
- 45865
- Product ID
- 45865-530_9adbe53e-3512-4013-e053-2a95a90a36d3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ciprofloxacin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Medsource Pharmaceuticals
- Application
- ANDA076639
- Marketing category
- ANDA
- Marketing start
- 2004-09-10
- Marketing end
- 0000-00-00
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 45865-530-14 | ciprofloxacin | 14 in 1 BOTTLE | TABLET | 14 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 45865-530 | CIPROFLOXACIN TABLET [MEDSOURCE PHARMACEUTICALS] | 1 | Legacy NDC, 1 package rows | 20191230_9adbfd58-04d8-0e4b-e053-2995a90a86bd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 45865-530-14 | 45865053014 | 14 TABLET in 1 BOTTLE (45865-530-14) | 14 tablet | 2018-12-12 | 0000-00-00 | No | No | Current |