NDC 15631-0029

AMMONIUM MURIATICUM

Ammonium Muriaticum

AMMONIUM MURIATICUM 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 Chloride.

Product ID15631-0029_fd38fedb-b216-45d0-9ca2-9ce8d39dfd6e
NDC15631-0029
Product TypeHuman Otc Drug
Proprietary NameAMMONIUM MURIATICUM
Generic NameAmmonium Muriaticum
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 CHLORIDE
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0029-1

200 PELLET in 1 PACKAGE (15631-0029-1)
Marketing Start Date2015-09-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0029-3 [15631002903]

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

NDC 15631-0029-5 [15631002905]

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

NDC 15631-0029-4 [15631002904]

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

NDC 15631-0029-2 [15631002902]

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

NDC 15631-0029-0 [15631002900]

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

NDC 15631-0029-1 [15631002901]

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

Drug Details

Active Ingredients

IngredientStrength
AMMONIUM CHLORIDE1 [hp_X]/1

OpenFDA Data

SPL SET ID:e43ce9da-2551-4dfd-9d59-99fb977b5353
Manufacturer
UNII

NDC Crossover Matching brand name "AMMONIUM MURIATICUM" or generic name "Ammonium Muriaticum"

NDCBrand NameGeneric Name
0220-0249Ammonium muriaticumAMMONIUM CHLORIDE
0220-0250Ammonium muriaticumAMMONIUM CHLORIDE
0220-0260Ammonium muriaticumAMMONIUM CHLORIDE
15631-0029AMMONIUM MURIATICUMAMMONIUM MURIATICUM
60512-6171AMMONIUM MURIATICUMAMMONIUM MURIATICUM
62106-4838AMMONIUM MURIATICUMAmmonium chloride
63545-003Ammonium MuriaticumAmmonium Muriaticum
63545-950Ammonium MuriaticumAmmonium Muriaticum
63545-951Ammonium MuriaticumAmmonium Muriaticum
63545-952Ammonium MuriaticumAmmonium Muriaticum
63545-953Ammonium MuriaticumAmmonium Muriaticum
63545-954Ammonium MuriaticumAmmonium Muriaticum
63545-955Ammonium MuriaticumAmmonium Muriaticum
68428-199Ammonium muriaticumAMMONIUM CHLORIDE
71919-045Ammonium muriaticumAMMONIUM CHLORIDE

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