Ciprofloxacin
- Product NDC
- 70934-623
- 11-digit product format
- 709340623
- Labeler code
- 70934
- Product ID
- 70934-623_ab6d21b6-2581-4b97-e053-2a95a90adc50
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA076794
- Marketing category
- ANDA
- Marketing start
- 2020-03-21
- Marketing end
- 0000-00-00
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 70934-623-20 | Ciprofloxacin | 20 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 20 | | 1 |
| 70934-623-30 | Ciprofloxacin | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70934-623 | CIPROFLOXACIN TABLET, FILM COATED [DENTON PHARMA, INC. DBA NORTHWIND PHARMACEUTICALS] | 1 | Legacy NDC, 2 package rows | 20201224_ab6d1d20-a4a3-a357-e053-2a95a90a6e1d.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 |
|---|
| 70934-623-20 | 70934062320 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-623-20) | 2020-04-01 | 0000-00-00 | No | No | Current |
| 70934-623-30 | 70934062330 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-623-30) | 2020-03-21 | 0000-00-00 | No | No | Current |