Ciprofloxacin
- Product NDC
- 67296-1097
- 11-digit product format
- 672961097
- Labeler code
- 67296
- Product ID
- 67296-1097_d60fd320-eb39-4489-e053-2995a90a8432
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA076558
- Marketing category
- ANDA
- Marketing start
- 2004-06-09
- 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
- 2023-12-31
- 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 |
|---|
| 67296-1097-1 | Ciprofloxacin | 10 in 1 BOTTLE | TABLET, FILM COATED | 10 | | 7 |
| 67296-1097-6 | Ciprofloxacin | 6 in 1 BOTTLE | TABLET, FILM COATED | 6 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1097 | CIPROFLOXACIN TABLET, FILM COATED [REDPHARM DRUG, INC.] | 7 | Legacy NDC, 2 package rows | 20240712_4e7bef83-aa63-3a6b-e054-00144ff88e88.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 |
|---|
| 67296-1097-1 | 67296109701 | 10 TABLET, FILM COATED in 1 BOTTLE (67296-1097-1) | 2004-06-09 | 0000-00-00 | No | No | Current |
| 67296-1097-6 | 67296109706 | 6 in 1 BOTTLE | | | | | Historical |