Home NDC 10797-720 NDC 10797-720 - BetaVet 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 10797-720
Package NDCs from labels 10797-720-01
Manufacturer American Regent, Inc.
Effective date 2024-10-07
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type BetaVet - American Regent, Inc. American Regent, Inc. 2024-10-07 PRESCRIPTION ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 10797-720-01 BetaVet 1 in 1 CARTON INJECTION, SUSPENSION 1 12 10797-720-01 BetaVet 5 mL in 1 VIAL INJECTION, SUSPENSION 5 12
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10797-720 BETAVET (BETAMETHASONE SODIUM PHOSPHATE AND BETAMETHASONE ACETATE) INJECTION, SUSPENSION [AMERICAN REGENT, INC.] 11 2 package rows 20241009_3eb6b1d3-4485-4b25-aaab-92de9b2fb322.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded BETAMETHASONE ACETATE ACTIVE INGREDIENT TI05AO53L7 BETAVET (BETAMETHASONE SODIUM PHOSPHATE AND BETAMETHASONE ACETATE) INJECTION, SUSPENSION [LUITPOLD PHARMACEUTICALS, INC.] 3 BETAMETHASONE SODIUM PHOSPHATE ACTIVE INGREDIENT 7BK02SCL3W BETAVET (BETAMETHASONE SODIUM PHOSPHATE AND BETAMETHASONE ACETATE) INJECTION, SUSPENSION [LUITPOLD PHARMACEUTICALS, INC.] 3 BETAMETHASONE ACTIVE MOIETY 9842X06Q6M BETAVET (BETAMETHASONE SODIUM PHOSPHATE AND BETAMETHASONE ACETATE) INJECTION, SUSPENSION [LUITPOLD PHARMACEUTICALS, INC.] 3 BENZALKONIUM CHLORIDE INACTIVE INGREDIENT F5UM2KM3W7 BETAVET (BETAMETHASONE SODIUM PHOSPHATE AND BETAMETHASONE ACETATE) INJECTION, SUSPENSION [LUITPOLD PHARMACEUTICALS, INC.] 3 EDETATE DISODIUM INACTIVE INGREDIENT 7FLD91C86K BETAVET (BETAMETHASONE SODIUM PHOSPHATE AND BETAMETHASONE ACETATE) INJECTION, SUSPENSION [LUITPOLD PHARMACEUTICALS, INC.] 3 SODIUM PHOSPHATE, DIBASIC, ANHYDROUS INACTIVE INGREDIENT 22ADO53M6F BETAVET (BETAMETHASONE SODIUM PHOSPHATE AND BETAMETHASONE ACETATE) INJECTION, SUSPENSION [LUITPOLD PHARMACEUTICALS, INC.] 3 SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE INACTIVE INGREDIENT 593YOG76RN BETAVET (BETAMETHASONE SODIUM PHOSPHATE AND BETAMETHASONE ACETATE) INJECTION, SUSPENSION [LUITPOLD PHARMACEUTICALS, INC.] 3 WATER INACTIVE INGREDIENT 059QF0KO0R BETAVET (BETAMETHASONE SODIUM PHOSPHATE AND BETAMETHASONE ACETATE) INJECTION, SUSPENSION [LUITPOLD PHARMACEUTICALS, INC.] 3
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 12 of 69 · 1,370 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.