FDA.reportPublic FDA data

NDC 76475-236-01 - CHLORTETRACYCLINE HYDROCHLORIDE

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
76475-236
Requested NDC
76475-236-01
Package NDCs from labels
76475-236-01
Manufacturer
Quo Vademus | Neogen Corporation - Mercer Rd. | Particle Technology Labs
Effective date
2023-11-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
CHLORTETRACYCLINE HYDROCHLORIDE - Quo Vademus | Neogen Corporation - Mercer Rd. | Particle Technology LabsQuo Vademus | Neogen Corporation - Mercer Rd. | Particle Technology Labs2023-11-08PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76475-236-01CHLORTETRACYCLINE HYDROCHLORIDE.726 kg in 1 POUCHPOWDER, FOR SOLUTION.7264
76475-236-01CHLORTETRACYCLINE HYDROCHLORIDE25 in 1 CARTONPOWDER, FOR SOLUTION254

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76475-236CHLORTETRACYCLINE HYDROCHLORIDE POWDER, FOR SOLUTION [QUO VADEMUS]42 package rows20231111_425503bf-1f04-4255-a2ba-b8fdd5584f0d.zip

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.