ciprofloxacin
- Product NDC
- 35356-846
- 11-digit product format
- 353560846
- Labeler code
- 35356
- Product ID
- 35356-846_8e9f9f94-1ae1-44f9-acce-6a7071129427
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ciprofloxacin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA076639
- Marketing category
- ANDA
- Marketing start
- 2004-09-10
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 35356-846-20 | 35356084620 | 20 TABLET in 1 BOTTLE (35356-846-20) | 20 tablet | 2004-09-10 | 0000-00-00 | No | No | Current |
| 35356-846-30 | 35356084630 | 30 TABLET in 1 BOTTLE (35356-846-30) | 30 tablet | 2004-09-10 | 0000-00-00 | No | No | Current |