Home NDC 0061-1355-01 NDC 0061-1355-01 - Aquaflor Type A Medicated Article 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 0061-1355
Requested NDC 0061-1355-01
Package NDCs from labels 0061-1355-01
Manufacturer Merck Sharp & Dohme Corp.
Effective date 2025-09-25
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Aquaflor ® (Florfenicol) Merck Sharp & Dohme Corp. 2025-09-25 VFD TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0061-1355-01 AquaflorType A Medicated Article 2 kg in 1 POUCH POWDER 2 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0061-1355 AQUAFLOR TYPE A MEDICATED ARTICLE (FLORFENICOL) POWDER [MERCK SHARP & DOHME CORP.] 9 1 package rows 20241024_03902b8d-4f0a-450c-9862-99576dd4ff67.zip
DailyMed Socrata Ingredients# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.