NDC 69036-110

LORTUSS LQ

Doxylamine Succinate, Pseudoephedrine Hydrochloride

LORTUSS LQ is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Sallus Laboratories, Llc. The primary component is Doxylamine Succinate; Pseudoephedrine Hydrochloride.

Product ID69036-110_67df3c55-a2b0-4185-8a0d-18754cdae920
NDC69036-110
Product TypeHuman Otc Drug
Proprietary NameLORTUSS LQ
Generic NameDoxylamine Succinate, Pseudoephedrine Hydrochloride
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2014-08-01
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart341
Labeler NameSallus Laboratories, LLC
Substance NameDOXYLAMINE SUCCINATE; PSEUDOEPHEDRINE HYDROCHLORIDE
Active Ingredient Strength6 mg/5mL; mg/5mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 69036-110-16

473 mL in 1 BOTTLE (69036-110-16)
Marketing Start Date2014-08-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69036-110-16 [69036011016]

LORTUSS LQ LIQUID
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitML
Marketing Start Date2014-08-01
Marketing End Date2019-12-31
Inactivation Date2019-11-27
Reactivation Date2020-05-13

Drug Details

Active Ingredients

IngredientStrength
DOXYLAMINE SUCCINATE6.25 mg/5mL

OpenFDA Data

SPL SET ID:cf3b8d12-8cba-433b-8cfb-93760dfa47e2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1094355
  • NDC Crossover Matching brand name "LORTUSS LQ" or generic name "Doxylamine Succinate, Pseudoephedrine Hydrochloride"

    NDCBrand NameGeneric Name
    69036-110LORTUSS LQDoxylamine Succinate, Pseudoephedrine Hydrochloride
    70868-750LORTUSS LQDoxylamine Succinate, Pseudoephedrine Hydrochloride

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