ciprofloxacin
- Product NDC
- 53002-7320
- 11-digit product format
- 530027320
- Labeler code
- 53002
- Product ID
- 53002-7320_2d432704-c743-41f1-a0d4-dfaa6957515f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA077568
- Marketing category
- ANDA
- Marketing start
- 2018-11-01
- Marketing end
- 0000-00-00
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 3 mg/mL
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-7320-2 | 53002732002 | 5 mL in 1 BOTTLE, DROPPER (53002-7320-2) | 5 ml | 2019-06-01 | 0000-00-00 | No | No | Current |