NDC 15631-0030

AMMONIUM PHOSPHORICUM

Ammonium Phosphoricum

AMMONIUM PHOSPHORICUM 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 Phosphate, Dibasic.

Product ID15631-0030_8d429218-2be7-4a38-b890-69901a749551
NDC15631-0030
Product TypeHuman Otc Drug
Proprietary NameAMMONIUM PHOSPHORICUM
Generic NameAmmonium Phosphoricum
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 PHOSPHATE, DIBASIC
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0030-0

100 PELLET in 1 PACKAGE (15631-0030-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0030-2 [15631003002]

AMMONIUM PHOSPHORICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0030-3 [15631003003]

AMMONIUM PHOSPHORICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0030-4 [15631003004]

AMMONIUM PHOSPHORICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0030-5 [15631003005]

AMMONIUM PHOSPHORICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0030-1 [15631003001]

AMMONIUM PHOSPHORICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0030-0 [15631003000]

AMMONIUM PHOSPHORICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

Drug Details

Active Ingredients

IngredientStrength
AMMONIUM PHOSPHATE, DIBASIC3 [hp_X]/1

OpenFDA Data

SPL SET ID:89f51cbd-4db6-4d25-8b1b-fd5b138c69b7
Manufacturer
UNII

NDC Crossover Matching brand name "AMMONIUM PHOSPHORICUM" or generic name "Ammonium Phosphoricum"

NDCBrand NameGeneric Name
0220-0268Ammonium phosphoricumAMMONIUM PHOSPHATE DIBASIC
15631-0030AMMONIUM PHOSPHORICUMAMMONIUM PHOSPHORICUM
60512-6173AMMONIUM PHOSPHORICUMAMMONIUM PHOSPHORICUM
63545-004Ammonium PhosphoricumAmmonium Phosphoricum
63545-956Ammonium PhosphoricumAmmonium Phosphoricum
63545-957Ammonium PhosphoricumAmmonium Phosphoricum
63545-958Ammonium PhosphoricumAmmonium Phosphoricum
63545-959Ammonium PhosphoricumAmmonium Phosphoricum
63545-960Ammonium PhosphoricumAmmonium Phosphoricum
63545-961Ammonium PhosphoricumAmmonium Phosphoricum
68428-200Ammonium phosphoricumAMMONIUM PHOSPHATE, DIBASIC
71919-046Ammonium phosphoricumAMMONIUM PHOSPHATE, DIBASIC

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