NDC 71919-098

Atropinum

Atropine

Atropinum is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Washington Homeopathic Products. The primary component is Atropine.

Product ID71919-098_7e395392-84bc-6c6c-e053-2a91aa0af863
NDC71919-098
Product TypeHuman Otc Drug
Proprietary NameAtropinum
Generic NameAtropine
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2010-02-03
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameWashington Homeopathic Products
Substance NameATROPINE
Active Ingredient Strength30 [hp_C]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71919-098-07

15 mL in 1 VIAL, GLASS (71919-098-07)
Marketing Start Date2010-02-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71919-098-09 [71919009809]

Atropinum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-03

NDC 71919-098-10 [71919009810]

Atropinum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-03

NDC 71919-098-07 [71919009807]

Atropinum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-03

NDC 71919-098-08 [71919009808]

Atropinum LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-02-03

Drug Details

Active Ingredients

IngredientStrength
ATROPINE30 [hp_C]/mL

OpenFDA Data

SPL SET ID:c1e821f8-43bd-4093-a33b-73fc1b1a6947
Manufacturer
UNII
UPC Code
  • 0740640241226
  • NDC Crossover Matching brand name "Atropinum" or generic name "Atropine"

    NDCBrand NameGeneric Name
    68428-237AtropinumATROPINE
    71919-098AtropinumATROPINE
    11704-101ATROPEN Auto-Injectoratropine
    11704-104ATROPEN Auto-Injectoratropine
    11704-105ATROPEN Auto-Injectoratropine
    11704-106ATROPEN Auto-Injectoratropine
    11704-107ATROPEN Auto-Injectoratropine

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