NDC 0363-9150

Wal-itin

Loratadine

Wal-itin is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Walgreens. The primary component is Loratadine.

Product ID0363-9150_b68ee76c-7dfc-4091-8e38-1504451f1ca4
NDC0363-9150
Product TypeHuman Otc Drug
Proprietary NameWal-itin
Generic NameLoratadine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2019-12-27
Marketing CategoryANDA / ANDA
Application NumberANDA075209
Labeler NameWalgreens
Substance NameLORATADINE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0363-9150-03

1 BOTTLE, PLASTIC in 1 BOX (0363-9150-03) > 30 TABLET in 1 BOTTLE, PLASTIC
Marketing Start Date2019-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0363-9150-45 [00363915045]

Wal-itin TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-12-27

NDC 0363-9150-03 [00363915003]

Wal-itin TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-12-27

NDC 0363-9150-70 [00363915070]

Wal-itin TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-12-27

NDC 0363-9150-05 [00363915005]

Wal-itin TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-12-27

NDC 0363-9150-30 [00363915030]

Wal-itin TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-12-27

NDC 0363-9150-20 [00363915020]

Wal-itin TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-12-27

NDC 0363-9150-15 [00363915015]

Wal-itin TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-12-27

NDC 0363-9150-10 [00363915010]

Wal-itin TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-12-27

NDC 0363-9150-90 [00363915090]

Wal-itin TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-12-27

Drug Details

Active Ingredients

IngredientStrength
LORATADINE10 mg/1

NDC Crossover Matching brand name "Wal-itin" or generic name "Loratadine"

NDCBrand NameGeneric Name
0363-0754Wal-itinLORATADINE
0363-1686WAL-ITINLORATADINE
0363-9150Wal-itinLoratadine
0363-9995Wal-itinWal-itin
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
0363-2085Wal-itin Allergy ReliefLoratadine

Trademark Results [Wal-itin]

Mark Image

Registration | Serial
Company
Trademark
Application Date
WAL-ITIN
WAL-ITIN
76478091 2803476 Live/Registered
Walgreen Co.
2002-12-24
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