Ciprofloxacin
- Product NDC
- 50090-4314
- 11-digit product format
- 500904314
- Labeler code
- 50090
- Product ID
- 50090-4314_71143abd-1c83-4c4e-bfed-8f402c467825
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076558
- Marketing category
- ANDA
- Marketing start
- 2004-06-09
- Marketing end
- 0000-00-00
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 500 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 |
|---|
| 50090-4314-0 | Ciprofloxacin | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | | 1 |
| 50090-4314-1 | Ciprofloxacin | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4314 | CIPROFLOXACIN TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 2 package rows | 20190611_cfc1963b-7a48-4129-b747-897a9d6de14c.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 |
|---|
| 50090-4314-0 | 50090431400 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-4314-0) | 2019-05-29 | 0000-00-00 | No | No | Current |
| 50090-4314-1 | 50090431401 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-4314-1) | 2019-05-29 | 0000-00-00 | No | No | Current |