NDC 71919-710

VESPA CRABRO

Vespa Crabro

VESPA CRABRO is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Vespa Crabro.

Product ID71919-710_99cca94c-1656-7e55-e053-2a95a90a2ca8
NDC71919-710
Product TypeHuman Otc Drug
Proprietary NameVESPA CRABRO
Generic NameVespa Crabro
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2011-05-17
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameWashington Homeopathic Products
Substance NameVESPA CRABRO
Active Ingredient Strength30 [hp_C]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71919-710-07

15 mL in 1 VIAL, GLASS (71919-710-07)
Marketing Start Date2011-05-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71919-710-08 [71919071008]

VESPA CRABRO LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-17

NDC 71919-710-09 [71919071009]

VESPA CRABRO LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-17

NDC 71919-710-07 [71919071007]

VESPA CRABRO LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-17

NDC 71919-710-10 [71919071010]

VESPA CRABRO LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2011-05-17

Drug Details

Active Ingredients

IngredientStrength
VESPA CRABRO30 [hp_C]/mL

NDC Crossover Matching brand name "VESPA CRABRO" or generic name "Vespa Crabro"

NDCBrand NameGeneric Name
0220-5254Vespa crabroVESPA CRABRO
68428-701Vespa crabroVESPA CRABRO
71919-710VESPA CRABROVESPA CRABRO
64117-299NAUSEAVESPA CRABRO

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.