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NDC 70518-2225-02 Amoxicillin and Clavulanate Potassium 875; 125 mg/1; mg/1 Details
Amoxicillin and Clavulanate Potassium 875; 125 mg/1; mg/1
Amoxicillin and Clavulanate Potassium is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is AMOXICILLIN; CLAVULANATE POTASSIUM.
Product Information
NDC | 70518-2225 |
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Product ID | 70518-2225_03241bf4-2d94-9933-e063-6394a90a435a |
Associated GPIs | 01990002200340 |
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 | Amoxicillin and Clavulanate Potassium |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Amoxicillin and Clavulanate Potassium |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET, FILM COATED |
Route | ORAL |
Active Ingredient Strength | 875; 125 |
Active Ingredient Units | mg/1; mg/1 |
Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
Labeler Name | REMEDYREPACK INC. |
Pharmaceutical Class | Penicillin-class Antibacterial [EPC], Penicillins [CS], beta Lactamase Inhibitor [EPC], beta Lactamase Inhibitors [MoA] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA091568 |
Listing Certified Through | 2024-12-31 |
Package
NDC 70518-2225-02 (70518222502)
NDC Package Code | 70518-2225-2 |
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Billing NDC | 70518222502 |
Package | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2225-2) |
Marketing Start Date | 2020-06-17 |
NDC Exclude Flag | N |
Pricing Information | N/A |