Quercus Rubra Glandium

Product NDC
37662-3299
11-digit product format
376623299
Labeler code
37662
Product ID
37662-3299_fd2ecde0-2970-060f-e053-6294a90afd98
Type
HUMAN OTC DRUG
Nonproprietary name
Quercus Rubra Glandium
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-06-02
Substance
QUERCUS RUBRA WHOLE
Active strength
200 [hp_C]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termMatched term
UQ0Z34X16UQUERCUS RUBRA WHOLEQUERCUS RUBRA WHOLE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-3299-137662329901200 PELLET in 1 VIAL, GLASS (37662-3299-1) 200 pellet2023-06-02NoNoHistorical
37662-3299-237662329902500 PELLET in 1 VIAL, GLASS (37662-3299-2) 500 pellet2023-06-02NoNoHistorical
37662-3299-3376623299033000 PELLET in 1 BOTTLE, GLASS (37662-3299-3) 3000 pellet2023-06-02NoNoHistorical
37662-3299-43766232990410000 PELLET in 1 BOTTLE, GLASS (37662-3299-4) 10000 pellet2023-06-02NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Quercus Rubra Glandium - Hahnemann Laboratories, INC.Hahnemann Laboratories, INC.2023-06-02HUMAN OTC DRUG LABEL1