NDC 71753-1152

Thymuline

Thymuline

Thymuline is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Ratis, Llc. The primary component is Nonathymulin.

Product ID71753-1152_b043481d-ce94-4d96-b738-1529d9c6cb7f
NDC71753-1152
Product TypeHuman Otc Drug
Proprietary NameThymuline
Generic NameThymuline
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2018-09-06
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRatis, LLC
Substance NameNONATHYMULIN
Active Ingredient Strength9 [hp_C]/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71753-1152-1

30 mL in 1 BOTTLE, SPRAY (71753-1152-1)
Marketing Start Date2018-09-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71753-1152-1 [71753115201]

Thymuline LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-09-06

Drug Details

Active Ingredients

IngredientStrength
NONATHYMULIN9 [hp_C]/mL

OpenFDA Data

SPL SET ID:8dfaeb98-df5b-4d18-95a8-07f6d7a4cfca
Manufacturer
UNII
UPC Code
  • 0371753115212
  • NDC Crossover Matching brand name "Thymuline" or generic name "Thymuline"

    NDCBrand NameGeneric Name
    61727-343ThymulineNONATHYMULIN
    71753-1052ThymulineThymuline
    71753-1152ThymulineThymuline

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