Home NDC 0061-8134 NDC 0061-8134 - Orbenin-DC This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 0061-8134
Package NDCs from labels 0061-8134-01, 0061-8134-06
Manufacturer Merck Sharp & Dohme Corp.
Effective date 2024-11-13
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0061-8134-01 Orbenin-DC 12 in 1 CARTON SUSPENSION 12 6 0061-8134-01 Orbenin-DC 7.5 mL in 1 SYRINGE SUSPENSION 7.5 6 0061-8134-06 Orbenin-DC 144 in 1 PAIL SUSPENSION 144 6 0061-8134-06 Orbenin-DC 7.5 mL in 1 SYRINGE SUSPENSION 7.5 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0061-8134 ORBENIN-DC (CLOXACILLIN BENZATHINE) SUSPENSION [MERCK SHARP & DOHME CORP.] 6 4 package rows 20241115_0fc4b59b-30b4-480f-bad9-460e30209a35.zip
DailyMed Socrata Ingredients# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.