Search by Drug Name or NDC
NDC 70518-2877-01 Penicillin V Potassium 500 mg/1 Details
Penicillin V Potassium 500 mg/1
Penicillin V 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 PENICILLIN V POTASSIUM.
MedlinePlus Drug Summary
Penicillin V potassium is used to treat certain infections caused by bacteria such as pneumonia and other respiratory tract infections, scarlet fever, and ear, skin, gum, mouth, and throat infections. It also is used to prevent rheumatic fever (a serious condition that may develop after a strep throat or scarlet fever infection and may cause swelling of the heart valves and other symptoms) from coming back. Penicillin V potassium is in a class of medications called penicillins. It works by killing bacteria. Antibiotics such as penicillin V potassium will not work for colds, flu, or other viral infections. Taking antibiotics when they are not needed increases your risk of getting an infection later that resists antibiotic treatment.
Related Packages: 70518-2877-01Last Updated: 05/05/2024
MedLinePlus Full Drug Details: Penicillin V Potassium
Product Information
| NDC | 70518-2877 |
|---|---|
| Product ID | 70518-2877_079f15aa-2ffc-e231-e063-6294a90a683b |
| 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 | Penicillin V Potassium |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Penicillin V Potassium |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 500 |
| Active Ingredient Units | mg/1 |
| Substance Name | PENICILLIN V POTASSIUM |
| Labeler Name | REMEDYREPACK INC. |
| Pharmaceutical Class | Penicillin-class Antibacterial [EPC], Penicillins [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA065435 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70518-2877-01 (70518287701)
| NDC Package Code | 70518-2877-1 |
|---|---|
| Billing NDC | 70518287701 |
| Package | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2877-1) |
| Marketing Start Date | 2023-09-08 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |