LORATADINE- loratadine tablet

Loratadine by

Drug Labeling and Warnings

Loratadine by is a Prescription medication manufactured, distributed, or labeled by Bryant Ranch Prepack. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT(S)

Active ingredient (in each tablet)
Loratadine USP, 10 mg

PURPOSE

Antihistamine

USE(S)

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

• runny nose:
  • itchy, watery eyes
• sneezing:
  • itching of the nose or throat

WARNINGS

DO NOT USE

if you have ever had an allergic reaction to this product or any of its ingredients.

ASK A DOCTOR BEFORE USE IF YOU HAVE

liver or kidney disease. Your doctor should determine if you need a different dose.

ASK A DOCTOR OR PHARMACIST BEFORE USE IF

WHEN USING THIS PRODUCT

do not take more than directed. Taking more than directed may cause drowsiness.

STOP USE AND ASK DOCTOR IF

an allergic reaction to this product occurs. Seek medical help right away.

PREGNANCY/BREASTFEEDING

ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS

• adults and children 6 years and over: 1 tablet daily; not more than 1 tablet in 24 hours
• children under 6 years of age: ask a doctor
• consumers with liver or kidney disease: ask a doctor

OTHER INFORMATION

Bottles:

• Tamper-evident: do not use if foil seal under cap, printed with "SEALED for YOUR PROTECTION" is missing, open or broken
• store between 20° to 25°C (68° to 77°F)

Blisters packs:

• safety sealed: do not use if the individual blister unit imprinted with loratadine is open or torn
• store between 20° to 25°C (68° to 77°F)
• protect from excessive moisture

INACTIVE INGREDIENTS

corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch

QUESTIONS OR COMMENTS?

Call 1-888-588-1418

HOW SUPPLIED

Loratadine USP, 10 mg: color white (White to Off white) and the imprint code is H;L20.

NDC: 71335-2551-1: 20 Tablets in a BOTTLE

NDC: 71335-2551-2: 30 Tablets in a BOTTLE

NDC: 71335-2551-3: 60 Tablets in a BOTTLE

NDC: 71335-2551-4: 14 Tablets in a BOTTLE

NDC: 71335-2551-5: 10 Tablets in a BOTTLE

NDC: 71335-2551-6: 90 Tablets in a BOTTLE

NDC: 71335-2551-7: 28 Tablets in a BOTTLE

NDC: 71335-2551-8: 15 Tablets in a BOTTLE

NDC: 71335-2551-9: 100 Tablets in a BOTTLE

Repackaged/Relabeled by:
Bryant Ranch Prepack, Inc.
Burbank, CA 91504

PRINCIPAL DISPLAY PANEL

Loratadine 10mg Tablet

INGREDIENTS AND APPEARANCE

LORATADINE  
loratadine tablet

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 71335-2551(NDC:69230-323)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)	LORATADINE	10 mg

Inactive Ingredients
Ingredient Name	Strength
STARCH, CORN (UNII: O8232NY3SJ)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	white (White to Off white)	Score	no score
Shape	ROUND	Size	6mm
Flavor		Imprint Code	H;L20
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71335-2551-1	20 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2025
2	NDC: 71335-2551-2	30 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2025
3	NDC: 71335-2551-3	60 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2025
4	NDC: 71335-2551-4	14 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2025
5	NDC: 71335-2551-5	10 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2025
6	NDC: 71335-2551-6	90 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2025
7	NDC: 71335-2551-7	28 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2025
8	NDC: 71335-2551-8	15 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2025
9	NDC: 71335-2551-9	100 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA211718	07/28/2023

Labeler - Bryant Ranch Prepack (171714327)

Registrant - Bryant Ranch Prepack (171714327)

Establishment
Name	Address	ID/FEI	Business Operations
Bryant Ranch Prepack		171714327	REPACK(71335-2551) , RELABEL(71335-2551)