NDC 15631-0027

AMMONIUM CARBONICUM

Ammonium Carbonicum

AMMONIUM CARBONICUM is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Ammonium Carbonate.

Product ID15631-0027_96b366cf-acee-4839-aca5-94fa089569c0
NDC15631-0027
Product TypeHuman Otc Drug
Proprietary NameAMMONIUM CARBONICUM
Generic NameAmmonium Carbonicum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-06
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameAMMONIUM CARBONATE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0027-0

100 PELLET in 1 PACKAGE (15631-0027-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0027-1 [15631002701]

AMMONIUM CARBONICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-06
Inactivation Date2020-01-31

NDC 15631-0027-0 [15631002700]

AMMONIUM CARBONICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-06
Inactivation Date2020-01-31

NDC 15631-0027-3 [15631002703]

AMMONIUM CARBONICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-06
Inactivation Date2020-01-31

NDC 15631-0027-2 [15631002702]

AMMONIUM CARBONICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-06
Inactivation Date2020-01-31

NDC 15631-0027-5 [15631002705]

AMMONIUM CARBONICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-06
Inactivation Date2020-01-31

NDC 15631-0027-4 [15631002704]

AMMONIUM CARBONICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-09-06
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
AMMONIUM CARBONATE3 [hp_X]/1

OpenFDA Data

SPL SET ID:4a812041-45e2-4f26-b0c7-670aa7cdcdb0
Manufacturer
UNII

NDC Crossover Matching brand name "AMMONIUM CARBONICUM" or generic name "Ammonium Carbonicum"

NDCBrand NameGeneric Name
0220-0241Ammonium carbonicumAMMONIUM CARBONATE
0220-0242Ammonium carbonicumAMMONIUM CARBONATE
0220-0248Ammonium carbonicumAMMONIUM CARBONATE
15631-0027AMMONIUM CARBONICUMAMMONIUM CARBONICUM
63545-933Ammonium CarbonicumAmmonium Carbonicum
63545-934Ammonium CarbonicumAmmonium Carbonicum
63545-935Ammonium CarbonicumAmmonium Carbonicum
63545-936Ammonium CarbonicumAmmonium Carbonicum
63545-939Ammonium CarbonicumAmmonium Carbonicum
63545-940Ammonium CarbonicumAmmonium Carbonicum
63545-941Ammonium CarbonicumAmmoniucm Carbonicum
63545-942Ammonium CarbonicumAmmonium Carbonicum
63545-943Ammonium CarbonicumAmmonium Carbonicum
68428-198Ammonium carbonicumAMMONIUM CARBONATE
71919-044Ammonium carbonicumAMMONIUM CARBONATE
69152-1053Ammonium carbonicum 200CAmmonium carbonicum

© 2021 FDA.report
This site is not affiliated with or endorsed by the FDA.