Home NDC 0220-0738 Belladonna
Product NDC 0220-0738
11-digit product format 002200738
Labeler code 0220
Product ID 0220-0738_f2f61a3b-d201-b356-e053-2995a90aa9d0
Type HUMAN OTC DRUG
Nonproprietary name ATROPA BELLADONNA
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance ATROPA BELLADONNA
Active strength 200 [kp_C]/200[kp_C]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Belladonna
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ATROPA BELLADONNA 200 [kp_C]/200[kp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination WQZ3G9PF0H 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 0220-0738-41 Belladonna 200 [kp_C] in 1 TUBE PELLET 200 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-0738 BELLADONNA (ATROPA BELLADONNA ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20230124_84ffe1b8-0fa0-0da1-e053-2a91aa0a30ed.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 Marketing start Marketing end Sample Exclude flag Status 0220-0738-41 00220073841 200 [kp_C] in 1 TUBE (0220-0738-41) 1983-03-03 0000-00-00 No No Current