Home NDC 37662-1308 Veratrum Album
Product NDC 37662-1308
11-digit product format 376621308
Labeler code 37662
Product ID 37662-1308_e5fafb25-a010-65ba-e053-2a95a90a4228
Type HUMAN OTC DRUG
Nonproprietary name Veratrum Album
Dosage form PELLET
Route ORAL
Labeler Hahnemann Laboratories, INC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2022-08-11
Substance VERATRUM ALBUM ROOT
Active strength 1 [hp_Q]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Veratrum Album
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength VERATRUM ALBUM ROOT 1 [hp_Q]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination QNS6W5US1Z 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 37662-1308-1 Veratrum Album 10000 in 1 BOTTLE, GLASS PELLET 10000 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37662-1308 VERATRUM ALBUM PELLET [HAHNEMANN LABORATORIES, INC.] 1 Current NDC, Legacy NDC, 1 package rows 20220813_e5fafb25-a00f-65ba-e053-2a95a90a4228.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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 37662-1308-1 37662130801 10000 PELLET in 1 BOTTLE, GLASS (37662-1308-1) 10000 pellet 2022-08-11 0000-00-00 No No Current