NDC 15631-0129

CHININUM SULPHURICUM

Chininum Sulphuricum

CHININUM SULPHURICUM 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 Quinine Sulfate.

Product ID15631-0129_4bb575f8-a81f-4184-9fb3-0550937f5b40
NDC15631-0129
Product TypeHuman Otc Drug
Proprietary NameCHININUM SULPHURICUM
Generic NameChininum Sulphuricum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameQUININE SULFATE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0129-0

100 PELLET in 1 PACKAGE (15631-0129-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0129-1 [15631012901]

CHININUM SULPHURICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0129-3 [15631012903]

CHININUM SULPHURICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0129-4 [15631012904]

CHININUM SULPHURICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0129-0 [15631012900]

CHININUM SULPHURICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0129-5 [15631012905]

CHININUM SULPHURICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

NDC 15631-0129-2 [15631012902]

CHININUM SULPHURICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-16

Drug Details

Active Ingredients

IngredientStrength
QUININE SULFATE3 [hp_X]/1

OpenFDA Data

SPL SET ID:61afa340-8f70-40d7-8946-25ce7b84d178
Manufacturer
UNII

NDC Crossover Matching brand name "CHININUM SULPHURICUM" or generic name "Chininum Sulphuricum"

NDCBrand NameGeneric Name
0220-1306Chininum sulphuricumQUININE SULFATE
0220-1307Chininum sulphuricumQUININE SULFATE
0220-1310Chininum sulphuricumQUININE SULFATE
0220-1311Chininum sulphuricumQUININE SULFATE
0220-1314Chininum sulphuricumQUININE SULFATE
0220-1325Chininum sulphuricumQUININE SULFATE
15631-0129CHININUM SULPHURICUMCHININUM SULPHURICUM
15631-0561CHININUM SULPHURICUMCHININUM SULPHURICUM
37662-0250Chininum SulphuricumChininum Sulphuricum
37662-0251Chininum SulphuricumChininum Sulphuricum
37662-0252Chininum SulphuricumChininum Sulphuricum
37662-0253Chininum SulphuricumChininum Sulphuricum
37662-0254Chininum SulphuricumChininum Sulphuricum
37662-0255Chininum SulphuricumChininum Sulphuricum
37662-0256Chininum SulphuricumChininum Sulphuricum
37662-0257Chininum SulphuricumChininum Sulphuricum
37662-0258Chininum SulphuricumChininum Sulphuricum
62106-5706CHININUM SULPHURICUMQuinine sulfate
66096-817Chininum SulphuricumCHININUM SULPHURICUM
68428-310Chininum sulphuricumQUININE SULFATE
71919-189Chininum sulphuricumQUININE SULFATE

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