Home NDC 0010-3017 NDC 0010-3017 - Ventipulmin 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 0010-3017
Package NDCs from labels 0010-3017-02, 0010-3017-03
Manufacturer Boehringer Ingelheim Animal Health USA Inc.
Effective date 2022-06-08
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Ventipulmin ® Syrup (clenbuterol HCl) Boehringer Ingelheim Animal Health USA Inc. 2022-06-08 PRESCRIPTION ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0010-3017-02 Ventipulmin 100 mL in 1 BOTTLE, PLASTIC SYRUP 100 6 0010-3017-02 Ventipulmin 1 in 1 CARTON SYRUP 1 6 0010-3017-03 Ventipulmin 330 mL in 1 BOTTLE, PLASTIC SYRUP 330 6 0010-3017-03 Ventipulmin 1 in 1 CARTON SYRUP 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0010-3017 VENTIPULMIN (CLENBUTEROL) SYRUP [BOEHRINGER INGELHEIM ANIMAL HEALTH USA INC.] 6 4 package rows 20220616_691e6c6a-0ac6-4cc2-bd87-954bf6716735.zip
DailyMed Socrata Ingredients# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.