ciprofloxacin
- Product NDC
- 50436-3135
- 11-digit product format
- 504363135
- Labeler code
- 50436
- Product ID
- 50436-3135_cad7a5ce-4dc3-42a9-b189-fd9201205c92
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ciprofloxacin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA076639
- Marketing category
- ANDA
- Marketing start
- 2004-09-10
- 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
- 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 |
|---|
| 50436-3135-3 | ciprofloxacin | 21 in 1 BOTTLE | TABLET | 21 | | 5 |
| 50436-3135-4 | ciprofloxacin | 10 in 1 BOTTLE | TABLET | 10 | | 5 |
| 50436-3135-5 | ciprofloxacin | 14 in 1 BOTTLE | TABLET | 14 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-3135 | CIPROFLOXACIN TABLET CIPROFLOXACIN TABLET [UNIT DOSE SERVICES] | 5 | Legacy NDC, 3 package rows | 20180110_a6181900-4a14-426c-80e9-c73f8a820514.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-3135-3 | 50436313503 | 21 in 1 BOTTLE | Historical |
| 50436-3135-4 | 50436313504 | 10 in 1 BOTTLE | Historical |
| 50436-3135-5 | 50436313505 | 14 in 1 BOTTLE | Historical |