Ciprofloxacin
- Product NDC
- 60687-947
- 11-digit product format
- 606870947
- Labeler code
- 60687
- Product ID
- 60687-947_5161db36-4cf5-589c-e063-6394a90ab75c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA077859
- Marketing category
- ANDA
- Marketing start
- 2026-05-03
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ciprofloxacin
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CIPROFLOXACIN HYDROCHLORIDE | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4BA73M5E37 |
| Rxcui | 309309 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60687-947-01 | Ciprofloxacin | 100 in 1 CARTON | TABLET, FILM COATED | 100 | | 1 |
| 60687-947-11 | Ciprofloxacin | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60687-947-01 | 60687094701 | 100 BLISTER PACK in 1 CARTON (60687-947-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-947-11) | 100 blister pack | 2026-05-03 | No | No | Historical |
| 60687-947-11 | 60687094711 | 1 in 1 BLISTER PACK | | | | | Historical |