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NDC 63629-1970-01 Vancomycin Hydrochloride 250 mg/5mL Details
Vancomycin Hydrochloride 250 mg/5mL
Vancomycin Hydrochloride is a ORAL POWDER, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is VANCOMYCIN HYDROCHLORIDE.
MedlinePlus Drug Summary
Vancomycin is used to treat colitis (inflammation of the intestine caused by certain bacteria) that may occur after antibiotic treatment. Vancomycin is in a class of medications called glycopeptide antibiotics. It works by killling bacteria in the intestines. Vancomycin will not kill bacteria or treat infections in any other part of the body when taken by mouth. Antibiotics such as vancomycin 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: 63629-1970-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Vancomycin
Product Information
| NDC | 63629-1970 |
|---|---|
| Product ID | 63629-1970_4c47f33a-d207-4eab-a67a-a1d99c1e9502 |
| Associated GPIs | 16280080102170 |
| GCN Sequence Number | 009333 |
| GCN Sequence Number Description | vancomycin HCl SOLN RECON 50 MG/ML ORAL |
| HIC3 | W1J |
| HIC3 Description | VANCOMYCIN ANTIBIOTICS AND DERIVATIVES |
| GCN | 41291 |
| HICL Sequence Number | 004042 |
| HICL Sequence Number Description | VANCOMYCIN HCL |
| Brand/Generic | Generic |
| Proprietary Name | Vancomycin Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Vancomycin Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | POWDER, FOR SOLUTION |
| Route | ORAL |
| Active Ingredient Strength | 250 |
| Active Ingredient Units | mg/5mL |
| Substance Name | VANCOMYCIN HYDROCHLORIDE |
| Labeler Name | Bryant Ranch Prepack |
| Pharmaceutical Class | Glycopeptide Antibacterial [EPC], Glycopeptides [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA061667 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 63629-1970-01 (63629197001)
| NDC Package Code | 63629-1970-1 |
|---|---|
| Billing NDC | 63629197001 |
| Package | 80 mL in 1 BOTTLE (63629-1970-1) |
| Marketing Start Date | 2019-09-09 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |