Ciprofloxacin
- Product NDC
- 70518-3035
- 11-digit product format
- 705183035
- Labeler code
- 70518
- Product ID
- 70518-3035_bc805a7b-7cb1-227b-e053-2995a90a98ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA208921
- Marketing category
- ANDA
- Marketing start
- 2021-03-01
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3035 | CIPROFLOXACIN TABLET, COATED [REMEDYREPACK INC.] | 6 | Legacy NDC | 20250409_1660dca3-0dda-42aa-bf34-44d4e420632c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3035-0 | 70518303500 | 30 TABLET, COATED in 1 BLISTER PACK (70518-3035-0) | 2021-03-01 | 0000-00-00 | No | No | Current |