NDC 71753-1052

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 ID71753-1052_12750478-181d-46eb-999c-56b7cd6a9205
NDC71753-1052
Product TypeHuman Otc Drug
Proprietary NameThymuline
Generic NameThymuline
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2017-10-03
Marketing End Date2023-01-05
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRatis, LLC
Substance NameNONATHYMULIN
Active Ingredient Strength9 [hp_C]/mL
NDC Exclude FlagN

Packaging

NDC 71753-1052-1

30 mL in 1 BOTTLE, SPRAY (71753-1052-1)
Marketing Start Date2017-10-03
Marketing End Date2023-01-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71753-1052-1 [71753105201]

Thymuline LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-10-03

Drug Details

Active Ingredients

IngredientStrength
NONATHYMULIN9 [hp_C]/mL

OpenFDA Data

SPL SET ID:076db039-764e-4696-8635-be750eca2281
Manufacturer
UNII
UPC Code
  • 0371753105213
  • NDC Crossover Matching brand name "Thymuline" or generic name "Thymuline"

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

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