Home NDC 85816-5022 BM Belladonna
Product NDC 85816-5022
11-digit product format 858165022
Labeler code 85816
Product ID 85816-5022_5c55a74d-2235-8f1b-e063-6394a90a2a47
Type HUMAN OTC DRUG
Nonproprietary name Belladonna
Dosage form GLOBULE
Route ORAL
Labeler BM Private Limited
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-01-01
Substance ATROPA BELLADONNA
Active strength 30 [hp_C]/g
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 BM Belladonna
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ATROPA BELLADONNA 30 [hp_C]/g
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85816-5022-1 BM Belladonna 30 g in 1 BOTTLE, GLASS GLOBULE 30 1
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 85816-5022-1 85816502201 30 g in 1 BOTTLE, GLASS (85816-5022-1) 30 g 2015-01-01 No No Current