NDC 63629-1329

Loratadine antihistamine

Loratadine

Loratadine antihistamine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Loratadine.

Product ID63629-1329_c4f306db-2e82-4c41-b6a1-b6008fc272f2
NDC63629-1329
Product TypeHuman Prescription Drug
Proprietary NameLoratadine antihistamine
Generic NameLoratadine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2008-10-15
Marketing CategoryANDA / ANDA
Application NumberANDA076301
Labeler NameBryant Ranch Prepack
Substance NameLORATADINE
Active Ingredient Strength10 mg/1
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 63629-1329-1

20 TABLET in 1 BOTTLE (63629-1329-1)
Marketing Start Date2022-02-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-1329-4 [63629132904]

Loratadine antihistamine TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-10-15
Inactivation Date2019-11-27

NDC 63629-1329-6 [63629132906]

Loratadine antihistamine TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-10-15
Inactivation Date2019-11-27

NDC 63629-1329-7 [63629132907]

Loratadine antihistamine TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-10-15
Inactivation Date2019-11-27

NDC 63629-1329-3 [63629132903]

Loratadine antihistamine TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-10-15
Inactivation Date2019-11-27

NDC 63629-1329-1 [63629132901]

Loratadine antihistamine TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-10-15
Inactivation Date2019-11-27

NDC 63629-1329-5 [63629132905]

Loratadine antihistamine TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-10-15
Inactivation Date2019-11-27

NDC 63629-1329-2 [63629132902]

Loratadine antihistamine TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-10-15
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
LORATADINE10 mg/1

OpenFDA Data

SPL SET ID:cd21751e-e62f-40f3-a254-f2db7cf9c101
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311372
  • NDC Crossover Matching brand name "Loratadine antihistamine" or generic name "Loratadine"

    NDCBrand NameGeneric Name
    68788-9080Loratadine antihistamineLoratadine antihistamine
    70518-0135Loratadine antihistamineLoratadine antihistamine
    70518-1335Loratadine antihistamineLoratadine antihistamine
    70518-1603Loratadine antihistamineLoratadine antihistamine
    0615-8217Loratadine antihistamineLoratadine antihistamine
    35356-881Loratadine antihistamineLoratadine antihistamine
    43353-259Loratadine antihistamineLoratadine antihistamine
    45802-650Loratadine antihistamineLoratadine antihistamine
    50090-0836Loratadine antihistamineLoratadine antihistamine
    50090-0837Loratadine antihistamineLoratadine antihistamine
    50436-3502Loratadine antihistamineLoratadine antihistamine
    50436-3501Loratadine antihistamineLoratadine antihistamine
    63187-601Loratadine antihistamineLoratadine antihistamine
    63629-1329Loratadine antihistamineLoratadine antihistamine
    66267-653Loratadine antihistamineLoratadine antihistamine
    70934-467Loratadine antihistamineLoratadine antihistamine
    0363-1612allergy reliefLoratadine
    0113-7612Basic Care allergy reliefLoratadine
    0113-7500basic care childrens allergy reliefloratadine
    0113-7671Basic Care Childrens Allergy ReliefLoratadine
    0121-0849Childrens LoratadineLORATADINE
    0363-2131Childrens LoratadineLoratadine
    0363-4020CHILDRENS LORATADINE ODTLoratadine
    0363-2092Childrens Wal-itinLoratadine
    0363-2108Childrens WalitinLoratadine
    0113-0612good sense allergy reliefLoratadine
    0113-1191good sense allergy reliefloratadine
    0113-1612good sense allergy reliefLoratadine
    0113-9755good sense allergy reliefloratadine
    0113-0671Good Sense childrens allergy reliefLoratadine
    0113-1019good sense childrens allergy reliefloratadine
    0113-1719good sense childrens allergy reliefLoratadine
    0363-0858Indoor Outdoor Allergy ReliefLoratadine
    0179-8317LoratadineLoratadine
    0363-0522LoratadineLoratadine
    0363-0527LoratadineLoratadine
    0363-0752LoratadineLoratadine
    0363-9603LoratadineLoratadine
    0363-0699Wal itinLoratadine
    0363-0754Wal-itinLORATADINE
    0363-1686WAL-ITINLORATADINE
    0363-9150Wal-itinLoratadine
    0363-2085Wal-itin Allergy ReliefLoratadine

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.