NDC 0220-5025

Titanium metallicum

Titanium

Titanium metallicum is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Boiron. The primary component is Titanium.

Product ID0220-5025_8773d0ab-e98b-eb41-e053-2995a90ad59c
NDC0220-5025
Product TypeHuman Otc Drug
Proprietary NameTitanium metallicum
Generic NameTitanium
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date1983-03-03
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameBoiron
Substance NameTITANIUM
Active Ingredient Strength30 [hp_C]/30[hp_C]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0220-5025-41

30 [hp_C] in 1 TUBE (0220-5025-41)
Marketing Start Date1983-03-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0220-5025-41 [00220502541]

Titanium metallicum PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date1983-03-03

Drug Details

Active Ingredients

IngredientStrength
TITANIUM30 [hp_C]/30[hp_C]

NDC Crossover Matching brand name "Titanium metallicum" or generic name "Titanium"

NDCBrand NameGeneric Name
0220-5025Titanium metallicumTITANIUM
15631-0445TITANIUM METALLICUMTITANIUM METALLICUM
37662-1277Titanium MetallicumTitanium Metallicum
37662-1278Titanium MetallicumTitanium Metallicum
37662-1279Titanium MetallicumTitanium Metallicum
37662-1280Titanium MetallicumTitanium Metallicum
37662-1281Titanium MetallicumTitanium Metallicum
37662-1282Titanium MetallicumTitanium Metallicum
37662-1283Titanium MetallicumTitanium Metallicum
37662-1284Titanium MetallicumTitanium Metallicum
68428-681Titanium metallicumTITANIUM
71919-683TITANIUM METALLICUMTitanium
64117-291NAUSEATITANIUM

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.