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NDC 63629-1326-02 Ciprofloxacin 250 mg/1 Details
Ciprofloxacin 250 mg/1
Ciprofloxacin is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is CIPROFLOXACIN HYDROCHLORIDE.
Product Information
| NDC | 63629-1326 |
|---|---|
| Product ID | 63629-1326_c5eb3888-b860-4599-8e3d-2b99b594a345 |
| Associated GPIs | 05000020100310 |
| GCN Sequence Number | 009509 |
| GCN Sequence Number Description | ciprofloxacin HCl TABLET 250 MG ORAL |
| HIC3 | W1Q |
| HIC3 Description | QUINOLONE ANTIBIOTICS |
| GCN | 47050 |
| HICL Sequence Number | 004124 |
| HICL Sequence Number Description | CIPROFLOXACIN HCL |
| Brand/Generic | Generic |
| Proprietary Name | Ciprofloxacin |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Ciprofloxacin |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 250 |
| Active Ingredient Units | mg/1 |
| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
| Labeler Name | Bryant Ranch Prepack |
| Pharmaceutical Class | Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA075593 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 63629-1326-02 (63629132602)
| NDC Package Code | 63629-1326-2 |
|---|---|
| Billing NDC | 63629132602 |
| Package | 10 TABLET, FILM COATED in 1 BOTTLE (63629-1326-2) |
| Marketing Start Date | 2005-06-27 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |