NDC 48951-7200

Mandragora Arnica

Mandragora Arnica

Mandragora Arnica is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy, Inc.. The primary component is Arnica Montana Whole; Betula Pubescens Leaf; Equisetum Arvense Top; Formica Rufa; Mandragora Officinarum Root; Sus Scrofa Meniscus.

Product ID48951-7200_dfb07548-ba83-15bb-e053-2a95a90a5043
NDC48951-7200
Product TypeHuman Otc Drug
Proprietary NameMandragora Arnica
Generic NameMandragora Arnica
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2009-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC /
Labeler NameUriel Pharmacy, Inc.
Substance NameARNICA MONTANA WHOLE; BETULA PUBESCENS LEAF; EQUISETUM ARVENSE TOP; FORMICA RUFA; MANDRAGORA OFFICINARUM ROOT; SUS SCROFA MENISCUS
Active Ingredient Strength15 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 48951-7200-1

10 AMPULE in 1 BOX (48951-7200-1) > 1 mL in 1 AMPULE
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Mandragora Arnica" or generic name "Mandragora Arnica"

NDCBrand NameGeneric Name
48951-7012Mandragora ArnicaMandragora Arnica
48951-7200Mandragora ArnicaMandragora Arnica

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