Home NDC 23243-0068-1 NDC 23243-0068-1 - CycleGuard 500 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 23243-0068
Requested NDC 23243-0068-1
Package NDCs from labels 23243-0068-1
Manufacturer Huvepharma, Inc
Effective date 2026-01-06
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type CycleGuard 500 - Huvepharma, Inc Huvepharma, Inc 2026-01-06 OTC TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 23243-0068-1 CycleGuard500 18 kg in 1 BOTTLE LIQUID 18 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 23243-0068 CYCLEGUARD 500 (MELENGESTROL ACETATE) LIQUID [HUVEPHARMA, INC] 2 1 package rows 20220518_3f843d3a-7250-4d3b-bd15-e8e32c9ddaae.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.