Ciprofloxacin
- Product NDC
- 61442-222
- 11-digit product format
- 614420222
- Labeler code
- 61442
- Product ID
- 61442-222_2d6a2060-1f59-696d-e063-6394a90a2796
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Carlsbad Technology, Inc.
- Application
- ANDA076126
- Marketing category
- ANDA
- Marketing start
- 2009-10-10
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ciprofloxacin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CIPROFLOXACIN HYDROCHLORIDE | 250 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4BA73M5E37 |
| Rxcui | 197511, 197512, 309309 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61442-222-01 | Ciprofloxacin | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 16 |
| 61442-222-10 | Ciprofloxacin | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | | 16 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| CIPROFLOXACIN HYDROCHLORIDE | ACTIVE INGREDIENT | 4BA73M5E37 | CIPROFLOXACIN TABLET, FILM COATED [CARLSBAD TECHNOLOGY, INC.] | 7 | |
| CIPROFLOXACIN | ACTIVE MOIETY | 5E8K9I0O4U | CIPROFLOXACIN TABLET, FILM COATED [CARLSBAD TECHNOLOGY, INC.] | 7 | |
| HYPROMELLOSE 2208 (15000 MPA.S) | INACTIVE INGREDIENT | Z78RG6M2N2 | CIPROFLOXACIN TABLET, FILM COATED [CARLSBAD TECHNOLOGY, INC.] | 7 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | CIPROFLOXACIN TABLET, FILM COATED [CARLSBAD TECHNOLOGY, INC.] | 7 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | CIPROFLOXACIN TABLET, FILM COATED [CARLSBAD TECHNOLOGY, INC.] | 7 | |
| MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) | INACTIVE INGREDIENT | 461P5CJN6T | CIPROFLOXACIN TABLET, FILM COATED [CARLSBAD TECHNOLOGY, INC.] | 7 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | CIPROFLOXACIN TABLET, FILM COATED [CARLSBAD TECHNOLOGY, INC.] | 7 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | CIPROFLOXACIN TABLET, FILM COATED [CARLSBAD TECHNOLOGY, INC.] | 7 | |
| TRIACETIN | INACTIVE INGREDIENT | XHX3C3X673 | CIPROFLOXACIN TABLET, FILM COATED [CARLSBAD TECHNOLOGY, INC.] | 7 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61442-222 | CIPROFLOXACIN (CIPROFLOXACIN HYDROCHLORIDE) TABLET, FILM COATED [CARLSBAD TECHNOLOGY, INC.] | 16 | Current NDC, Legacy NDC, 2 package rows | 20250207_37527eca-115e-4582-88cd-bba851ac6069.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61442-222-01 | 61442022201 | 100 TABLET, FILM COATED in 1 BOTTLE (61442-222-01) | 2009-10-10 | 0000-00-00 | No | No | Current |
| 61442-222-10 | 61442022210 | 1000 TABLET, FILM COATED in 1 BOTTLE (61442-222-10) | 2009-10-10 | 0000-00-00 | No | No | Current |