NDC 69152-1032

Pulsatilla 200C

Pulsatilla

Pulsatilla 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 Pulsatilla Vulgaris.

Product ID69152-1032_318be153-c514-5b85-e054-00144ff8d46c
NDC69152-1032
Product TypeHuman Otc Drug
Proprietary NamePulsatilla 200C
Generic NamePulsatilla
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-06-11
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameParamesh Banerji Life Sciences LLC
Substance NamePULSATILLA VULGARIS
Active Ingredient Strength200 [hp_C]/1
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 69152-1032-1

96 PELLET in 1 BOTTLE (69152-1032-1)
Marketing Start Date2015-06-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69152-1032-1 [69152103201]

Pulsatilla 200C PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-06-11
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
PULSATILLA VULGARIS200 [hp_C]/1

OpenFDA Data

SPL SET ID:183935e8-6182-545b-e054-00144ff8d46c
Manufacturer
UNII

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

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