ciprofloxacin
- Product NDC
- 55700-737
- 11-digit product format
- 557000737
- Labeler code
- 55700
- Product ID
- 55700-737_dba1f762-8ef6-4efd-abf6-45c37ff04b03
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- Quality Care Products, LLC
- Application
- ANDA077568
- Marketing category
- ANDA
- Marketing start
- 2019-03-29
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55700-737 | CIPROFLOXACIN SOLUTION [QUALITY CARE PRODUCTS, LLC] | 3 | Legacy NDC | 20241220_8e63c1ce-2848-4ff9-8705-fdf8e20bdb02.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-737-05 | 55700073705 | 1 BOTTLE, PLASTIC in 1 CARTON (55700-737-05) > 5 mL in 1 BOTTLE, PLASTIC | 2019-03-29 | 0000-00-00 | No | No | Current |