Home NDC 65090-001 NDC 65090-001 - AniHist 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 65090-001
Package NDCs from labels 65090-001-15, 65090-001-30
Manufacturer AHC Products Inc | Delta Synthetic Co., Ltd. | Supriya Lifescience Ltd.
Effective date 2022-01-21
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Drug Facts AHC Products Inc | Delta Synthetic Co., Ltd. | Supriya Lifescience Ltd. 2022-01-21 OTC ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 65090-001-15 AniHist 566 g in 1 JAR GRANULE 566 117 65090-001-30 AniHist 2264 g in 1 PAIL GRANULE 2264 117
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 65090-001 ANIHIST (GUAFENESIN AND PYRILAMINE MALEATE) GRANULE [AHC PRODUCTS INC] 117 2 package rows 20220203_c54f1636-bb8c-4181-a6d5-14ab1c8a47fd.zip
DailyMed Socrata Ingredients#