Ciprofloxacin
- Product NDC
- 55700-884
- 11-digit product format
- 557000884
- Labeler code
- 55700
- Product ID
- 55700-884_98d1f7b9-e9d2-4570-8f06-4782d2d7bc83
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA077859
- Marketing category
- ANDA
- Marketing start
- 2020-10-06
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-884-06 | 55700088406 | 6 TABLET, FILM COATED in 1 BOTTLE (55700-884-06) | 2020-10-06 | 0000-00-00 | No | No | Current |
| 55700-884-10 | 55700088410 | 10 TABLET, FILM COATED in 1 BOTTLE (55700-884-10) | 2020-12-07 | 0000-00-00 | No | No | Current |