NDC 0363-0725

Loratadine and Pseudoephedrine

Loratadine And Pseudoephedrine

Loratadine and Pseudoephedrine is a Oral Tablet, Film Coated, Extended Release in the Human Otc Drug category. It is labeled and distributed by Walgreen Company. The primary component is Loratadine; Pseudoephedrine Sulfate.

Product ID0363-0725_0c2d87ca-fff0-46d5-9800-756693969a77
NDC0363-0725
Product TypeHuman Otc Drug
Proprietary NameLoratadine and Pseudoephedrine
Generic NameLoratadine And Pseudoephedrine
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2013-11-07
Marketing CategoryANDA / ANDA
Application NumberANDA076557
Labeler NameWalgreen Company
Substance NameLORATADINE; PSEUDOEPHEDRINE SULFATE
Active Ingredient Strength10 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0363-0725-15

1 BLISTER PACK in 1 CARTON (0363-0725-15) > 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Marketing Start Date2013-11-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0363-0725-56 [00363072556]

Loratadine and Pseudoephedrine TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076557
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-11-07
Inactivation Date2020-01-31

NDC 0363-0725-15 [00363072515]

Loratadine and Pseudoephedrine TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076557
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2013-11-07
Inactivation Date2020-01-31

NDC 0363-0725-69 [00363072569]

Loratadine and Pseudoephedrine TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA076557
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2013-11-07
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
LORATADINE10 mg/1

OpenFDA Data

SPL SET ID:ab7e4406-997a-43be-af99-a07a2da870da
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1117562
  • NDC Crossover Matching brand name "Loratadine and Pseudoephedrine" or generic name "Loratadine And Pseudoephedrine"

    NDCBrand NameGeneric Name
    0363-0725Loratadine and PseudoephedrineLoratadine and Pseudoephedrine
    11822-9990Loratadine and PseudoephedrineLORATADINE and PSEUDOEPHEDRINE SULFATE
    21695-729Loratadine and Pseudoephedrineloratadine and pseudoephedrine
    41163-165Loratadine and PseudoephedrineLoratadine and Pseudoephedrine
    46122-383Loratadine and Pseudoephedrineloratadine and pseudoephedrine
    51660-488Loratadine and Pseudoephedrineloratadine and pseudoephedrine
    51660-491Loratadine and Pseudoephedrineloratadine and pseudoephedrine
    51660-724Loratadine and Pseudoephedrineloratadine and pseudoephedrine
    61715-016Loratadine and PseudoephedrineLoratadine and Pseudoephedrine
    63187-305Loratadine and Pseudoephedrineloratadine and pseudoephedrine
    63629-7766Loratadine and Pseudoephedrineloratadine and pseudoephedrine
    70518-0653Loratadine and Pseudoephedrineloratadine and pseudoephedrine
    59779-726ALLERGY RELIEF-DLoratadine and Pseudoephedrine

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