NDC 17030-101 - Folltropin

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
17030-101
Package NDCs from labels
17030-101-70
Manufacturer
Vetoquinol USA, Inc. | Jubilant HollisterStier General Partnership | Vetoquinol N.-A. INC | Nucro-Technics | Neopharm Labs Inc.
Effective date
2020-12-17
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
FOLLTROPIN ® [porcine pituitary-derived follicle stimulating hormone for injection]Vetoquinol USA, Inc. | Jubilant HollisterStier General Partnership | Vetoquinol N.-A. INC | Nucro-Technics | Neopharm Labs Inc.2020-12-17PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17030-101-70Folltropin1 in 1 CARTONKIT15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17030-101FOLLTROPIN (FOLLICLE STIMULATING HORMONE (PORCINE)) KIT [VETOQUINOL USA, INC.]51 package rows20201222_88a149f0-8a44-48d1-a5df-35b1fd1559a1.zip

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 53 of 53 · 1,042 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RingersSODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE,Baxter Healthcare Corporatione1953d54-818d-46a6-8532-518ebae6d84e2012-06-13Exact identifier
unii: 451W47IQ8X
Lactated RingersSODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDEBaxter Healthcare Corporationf09f80bf-2f8b-4420-865d-aec2d5e5cd4d2012-06-12Exact identifier
unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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