Ciprofloxacin
- Product NDC
- 50436-0714
- 11-digit product format
- 504360714
- Labeler code
- 50436
- Product ID
- 50436-0714_d7c98e0b-33be-45c8-9e12-79ed352efbc7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Unit Dose Services
- Application
- ANDA076555
- Marketing category
- ANDA
- Marketing start
- 2009-07-24
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-0714-1 | Ciprofloxacin | 5 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 5 | | 2 |
| 50436-0714-1 | Ciprofloxacin | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0714 | CIPROFLOXACIN (CIPROFLOXACIN HYDROCHLORIDE) SOLUTION/ DROPS [UNIT DOSE SERVICES] | 2 | Legacy NDC, 2 package rows | 20180810_0d6b023f-6296-4567-b0f0-819eaefbfdc5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 50436-0714-1 | 50436071401 | 5 mL in 1 BOTTLE, DROPPER | 5 ml | Historical |