Home NDC 63545-959-01 Ammonium Phosphoricum
Product NDC 63545-959
Requested package NDC 63545-959-01
11-digit product format 635450959
Labeler code 63545
Product ID 63545-959_2b49322a-dc24-f4a1-e063-6294a90a6cff
Type HUMAN OTC DRUG
Nonproprietary name Ammonium Phosphoricum
Dosage form PELLET
Route ORAL
Labeler Hahnemann Laboratories, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2020-10-23
Substance AMMONIUM PHOSPHATE, DIBASIC
Active strength 200 [hp_C]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 3 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 63545-959 63545-959-01 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 63545-959 63545-959-01 I Inactivated by FDA excluded / ndc_excluded.zip 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 63545-959 63545-959-01 I Inactivated by FDA excluded / ndc_excluded.zip bd6a592717d7…303034d00443…
Additional Listing Data#
Finished product Yes
Brand name base Ammonium Phosphoricum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AMMONIUM PHOSPHATE, DIBASIC 200 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 10LGE70FSU Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63545-959-01 Ammonium Phosphoricum 200 in 1 VIAL, GLASS PELLET 200 3 63545-959-02 Ammonium Phosphoricum 500 in 1 VIAL, GLASS PELLET 500 3 63545-959-03 Ammonium Phosphoricum 3000 in 1 BOTTLE, GLASS PELLET 3000 3 63545-959-04 Ammonium Phosphoricum 10000 in 1 BOTTLE, GLASS PELLET 10000 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63545-959 AMMONIUM PHOSPHORICUM PELLET [HAHNEMANN LABORATORIES, INC.] 3 Current NDC, Legacy NDC, 4 package rows 20250112_b25e39bd-7e81-1ef1-e053-2995a90a6d82.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 63545-959-01 63545095901 200 PELLET in 1 VIAL, GLASS (63545-959-01) 200 pellet 2020-10-23 0000-00-00 No No Current