Ciprofloxacin
- Product NDC
- 0615-8147
- 11-digit product format
- 006158147
- Labeler code
- 0615
- Product ID
- 0615-8147_50fd2137-176c-494a-a801-dd8cc38bb2b1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA075593
- Marketing category
- ANDA
- Marketing start
- 2004-06-09
- Marketing end
- 2022-04-30
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0615-8147-14 | 00615814714 | 14 TABLET, FILM COATED in 1 BLISTER PACK (0615-8147-14) | 2019-06-06 | 2022-04-30 | No | No | Current |