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NDC 70934-0038-91 Amoxicillin 875 mg/1 Details
Amoxicillin 875 mg/1
Amoxicillin is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is AMOXICILLIN.
MedlinePlus Drug Summary
Amoxicillin is used to treat certain infections caused by bacteria, such as pneumonia; bronchitis (infection of the airway tubes leading to the lungs); and infections of the ears, nose, throat, urinary tract, and skin. It is also used in combination with other medications to eliminate H. pylori, a bacteria that causes ulcers. Amoxicillin is in a class of medications called penicillin-like antibiotics. It works by stopping the growth of bacteria. Antibiotics such as amoxicillin will not work for colds, flu, and other viral infections. Taking antibiotics when they are not needed increases your risk of getting an infection later that resists antibiotic treatment.
Related Packages: 70934-0038-91Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Amoxicillin
Product Information
| NDC | 70934-0038 |
|---|---|
| Product ID | 70934-038_ff48f0bd-7144-d34a-e053-6294a90a3c1d |
| Associated GPIs | 01200010100315 |
| GCN Sequence Number | 040292 |
| GCN Sequence Number Description | amoxicillin TABLET 875 MG ORAL |
| HIC3 | W1A |
| HIC3 Description | PENICILLIN ANTIBIOTICS |
| GCN | 39632 |
| HICL Sequence Number | 003963 |
| HICL Sequence Number Description | AMOXICILLIN |
| Brand/Generic | Generic |
| Proprietary Name | Amoxicillin |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Amoxicillin |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 875 |
| Active Ingredient Units | mg/1 |
| Substance Name | AMOXICILLIN |
| Labeler Name | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
| Pharmaceutical Class | Penicillin-class Antibacterial [EPC], Penicillins [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA065256 |
| Listing Certified Through | n/a |
Package
NDC 70934-0038-91 (70934003891)
| NDC Package Code | 70934-038-91 |
|---|---|
| Billing NDC | 70934003891 |
| Package | 20 TABLET, FILM COATED in 1 DOSE PACK (70934-038-91) |
| Marketing Start Date | 2017-10-31 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |