Home NDC 0220-0250 Ammonium muriaticum
Product NDC 0220-0250
11-digit product format 002200250
Labeler code 0220
Product ID 0220-0250_0410a1fe-a4cb-1f65-e063-6294a90ac687
Type HUMAN OTC DRUG
Nonproprietary name AMMONIUM CHLORIDE
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance AMMONIUM CHLORIDE
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 Ammonium muriaticum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AMMONIUM CHLORIDE 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 01Q9PC255D Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0220-0250-41 Ammonium muriaticum 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 0220-0250 AMMONIUM MURIATICUM (AMMONIUM CHLORIDE ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20230830_84b58da5-40e4-f3c1-e053-2991aa0aeb82.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 0220-0250-41 00220025041 200 [kp_C] in 1 TUBE (0220-0250-41) 1983-03-03 0000-00-00 No No Current