NDC 69152-1011

Sepia 200C

Sepia

Sepia 200C is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Paramesh Banerji Life Sciences Llc. The primary component is Sepia Officinalis Juice.

Product ID69152-1011_3566918d-76fb-68b3-e054-00144ff88e88
NDC69152-1011
Product TypeHuman Otc Drug
Proprietary NameSepia 200C
Generic NameSepia
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-06-04
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameParamesh Banerji Life Sciences LLC
Substance NameSEPIA OFFICINALIS JUICE
Active Ingredient Strength200 [hp_C]/1
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 69152-1011-1

96 PELLET in 1 BOTTLE (69152-1011-1)
Marketing Start Date2015-06-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69152-1011-1 [69152101101]

Sepia 200C PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-06-04
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
SEPIA OFFICINALIS JUICE200 [hp_C]/1

OpenFDA Data

SPL SET ID:17ad7e94-147d-67bb-e054-00144ff88e88
Manufacturer
UNII

NDC Crossover Matching brand name "Sepia 200C" or generic name "Sepia"

NDCBrand NameGeneric Name
69152-1011Sepia 200CSepia
0295-2600FungicureSepia
52389-226FungicureSepia
52389-666FungicureSepia
61727-054Menopause Relief Homeopathic RemedySepia
0360-0342SEPIASEPIA
0360-0343SEPIASEPIA
15631-0402SEPIASEPIA
15631-0684SEPIASEPIA
37662-2097SepiaSepia
37662-2098SepiaSepia
37662-2099SepiaSepia
37662-2100SepiaSepia
37662-2101SepiaSepia
37662-2102SepiaSepia
37662-2103SepiaSepia
37662-2104SepiaSepia
37662-2105SepiaSepia
44911-0391SepiaSepia
53499-5933SepiaSepia
53499-5971SepiaSepia
53645-1561SepiaSepia
55714-6490SepiaSepia
57520-0368SepiaSepia
60512-1043SEPIASEPIA
62106-6718SEPIASepia
63083-7134SepiaSepia
76472-3033SEPIASEPIA
69152-1187Sepia 6CSepia
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