Home NDC 84761-0007 MEnera
Product NDC 84761-0007
11-digit product format 847610007
Labeler code 84761
Product ID 84761-0007_590e8ddd-141b-6e9c-e063-6294a90a1082
Type HUMAN OTC DRUG
Nonproprietary name MEnera
Dosage form CAPSULE
Route ORAL
Labeler Tejeda Enterprises Incorporated
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2024-10-01
Substance ALLICIN; UBIQUINOL; LEPIDIUM MEYENII ROOT
Active strength 1200; 200; 700 mg/2U; mg/2U; mg/2U
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base MEnera
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALLICIN 1200 mg/2U UBIQUINOL 200 mg/2U LEPIDIUM MEYENII ROOT 700 mg/2U
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3C39BY17Y6 Internal UNII lookup M9NL0C577Y Internal UNII lookup HP7119212T Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84761-0007-1 84761000701 60 U in 1 CAPSULE (84761-0007-1) 60 u 2024-10-01 No No Current