Ciprofloxacin
- Product NDC
- 0615-8367
- 11-digit product format
- 006158367
- Labeler code
- 0615
- Product ID
- 0615-8367_914948ba-52db-4a62-8b47-a0dc43047d76
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0615-8367-14 | 00615836714 | 14 TABLET, FILM COATED in 1 BLISTER PACK (0615-8367-14) | 2020-12-11 | 0000-00-00 | No | No | Current |