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NDC 70518-3215-03 Cefuroxime Axetil 500 mg/1 Details
Cefuroxime Axetil 500 mg/1
Cefuroxime Axetil is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is CEFUROXIME AXETIL.
Product Information
| NDC | 70518-3215 |
|---|---|
| Product ID | 70518-3215_09052efb-4b0d-2e52-e063-6294a90a9d84 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Cefuroxime Axetil |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Cefuroxime Axetil |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 500 |
| Active Ingredient Units | mg/1 |
| Substance Name | CEFUROXIME AXETIL |
| Labeler Name | REMEDYREPACK INC. |
| Pharmaceutical Class | Cephalosporin Antibacterial [EPC], Cephalosporins [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA065308 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70518-3215-03 (70518321503)
| NDC Package Code | 70518-3215-3 |
|---|---|
| Billing NDC | 70518321503 |
| Package | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3215-3) |
| Marketing Start Date | 2023-10-30 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |