Home NDC 48951-8438 Prostata 8X
Product NDC 48951-8438
11-digit product format 489518438
Labeler code 48951
Product ID 48951-8438_42f49022-cde0-a70e-e063-6394a90a8b69
Type HUMAN OTC DRUG
Nonproprietary name Prostata 8X
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance BOS TAURUS PROSTATE GLAND
Active strength 8 [hp_X]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Prostata 8X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BOS TAURUS PROSTATE GLAND 8 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1P66FXU2MW Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-8438-1 Prostata 8X 10 in 1 BOX LIQUID 10 4 48951-8438-1 Prostata 8X 1 mL in 1 AMPULE LIQUID 1 4
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 48951-8438-1 48951843801 10 AMPULE in 1 BOX (48951-8438-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 No No Current