NDC 69152-1190

Pulsatilla 6C

Pulsatilla

Pulsatilla 6C 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 Pulsatilla Vulgaris.

Product ID69152-1190_331dd35f-682d-0ce8-e054-00144ff8d46c
NDC69152-1190
Product TypeHuman Otc Drug
Proprietary NamePulsatilla 6C
Generic NamePulsatilla
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-06-19
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameParamesh Banerji Life Sciences LLC
Substance NamePULSATILLA VULGARIS
Active Ingredient Strength6 [hp_C]/1
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 69152-1190-1

96 PELLET in 1 BOTTLE (69152-1190-1)
Marketing Start Date2015-06-19
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69152-1190-1 [69152119001]

Pulsatilla 6C PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-06-19
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
PULSATILLA VULGARIS6 [hp_C]/1

OpenFDA Data

SPL SET ID:18d8e6a9-c03f-1988-e054-00144ff8d46c
Manufacturer
UNII

NDC Crossover Matching brand name "Pulsatilla 6C" or generic name "Pulsatilla"

NDCBrand NameGeneric Name
69152-1190Pulsatilla 6CPulsatilla
15631-0357PULSATILLAPULSATILLA
15631-0661PULSATILLAPULSATILLA
53645-1980PulsatillaPulsatilla
53645-1981PulsatillaPulsatilla
53645-2130PulsatillaPulsatilla
55714-6440PulsatillaPulsatilla
57556-017PulsatillaPulsatilla
60512-1039PULSATILLAPULSATILLA
63083-7131PulsatillaPulsatilla
76472-3030PulsatillaPulsatilla
43406-0258Pulsatilla 200CPulsatilla
69152-1032Pulsatilla 200CPulsatilla
69152-1005Pulsatilla 30CPulsatilla
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.