NDC 44911-0476 – Adrenapar

American Ginseng 3 [hp_X]/mL; Avena Sativa Flowering Top 3 [hp_X]/mL; Sus Scrofa Adrenal Gland 8 [hp_X]/mL; Arsenic Triiodide 12 [hp_X]/mL; Strychnos Ignatii… · Liquid · Oral

Human Otc Drug

Product NDC44911-0476

Product details

Brand name
Adrenapar
Generic name
Aralia Quinquefolia, Avena Sativa, Glandula Suprarenalis Suis, Arsenicum Iodatum, Ignatia Amara, Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Zincum Metallicum
Labeler
Energique, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
September 26, 2018
Marketing end
August 30, 2027
Pharmacologic class
Non-Standardized Plant Allergenic Extract

Active ingredients

Uses, dosage, side effects and warnings for Adrenapar →

Package NDC codes (1)

Package NDCDescriptionSince
44911-0476-130 mL in 1 BOTTLE, DROPPER (44911-0476-1)Sep 26, 2018

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