Ciprofloxacin
- Product NDC
- 36000-008
- 11-digit product format
- 360000008
- Labeler code
- 36000
- Product ID
- 36000-008_5a51028b-06c4-4160-9165-8fc08d11b29d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Baxter Healthcare Corporation
- Application
- ANDA078024
- Marketing category
- ANDA
- Marketing start
- 2008-08-04
- Marketing end
- 0000-00-00
- Substance
- CIPROFLOXACIN
- Active strength
- 2 mg/mL
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 36000-008-24 | 36000000824 | 100 mL in 1 BAG (36000-008-24) | 100 ml | 2008-08-04 | 0000-00-00 | No | No | Current |