Loratadine by Bryant Ranch Prepack LORATADINE tablet

Loratadine by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient (in each tablet)

Loratadine, USP 10 mg

Purpose

Antihistamine

Uses

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.

When using this product

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

Stop use and ask a doctor

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

If pregnant or breast-feeding,

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

• Safety sealed: do not use if the imprinted bottle seal is open or torn (for bottle only).

• Store at 20°-25°C (68°-77°F) (see USP Controlled Room Temperature).

Inactive Ingredients

Lactose monohydrate, magnesium stearate, microcrystalline cellulose and sodium starch glycolate.

Questions or comments?

1-800-525-8747

10-2015M

Sandoz Inc.

Princeton, NJ 08540

HOW SUPPLIED

Product: 71335-0751

NDC: 71335-0751-1 20 TABLET in a BOTTLE

NDC: 71335-0751-2 30 TABLET in a BOTTLE

NDC: 71335-0751-3 60 TABLET in a BOTTLE

NDC: 71335-0751-4 14 TABLET in a BOTTLE

NDC: 71335-0751-5 10 TABLET in a BOTTLE

NDC: 71335-0751-6 90 TABLET in a BOTTLE

NDC: 71335-0751-7 28 TABLET in a BOTTLE

NDC: 71335-0751-8 15 TABLET in a BOTTLE

NDC: 71335-0751-9 100 TABLET in a BOTTLE

Loratadine 10mg Tablet

INGREDIENTS AND APPEARANCE

LORATADINE 
loratadine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71335-0751(NDC:0781-5077)
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
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)

Product Characteristics
Color	WHITE (white to off white)	Score	no score
Shape	ROUND	Size	6mm
Flavor		Imprint Code	GG296
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71335-0751-9	100 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2003
2	NDC: 71335-0751-1	20 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2003
3	NDC: 71335-0751-4	14 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2003
4	NDC: 71335-0751-7	28 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2003
5	NDC: 71335-0751-2	30 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2003
6	NDC: 71335-0751-8	15 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2003
7	NDC: 71335-0751-5	10 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2003
8	NDC: 71335-0751-6	90 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2003
9	NDC: 71335-0751-3	60 in 1 BOTTLE; Type 0: Not a Combination Product	01/21/2003

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA075209	01/21/2003

Labeler - Bryant Ranch Prepack (171714327)

Establishment
Name	Address	ID/FEI	Business Operations
Bryant Ranch Prepack		171714327	REPACK(71335-0751) , RELABEL(71335-0751)