IBUPROFEN- ibuprofen tablet 
Granules India Limited

----------

Ibuprofen Tablets, USP 200 mg

Drug Facts

ACTIVE INGREDIENT (in each tablet/caplet)

Ibuprofen 200 mg (NSAID) *

nonsteroidal anti-inflammatory drug

PURPOSE

Pain reliever/ fever reducer

USES

WARNINGS

Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin.

Symptoms may include:

If an allergic reaction occurs, stop use and seek medical help right away.

Stomach bleeding warning

This product contains an NSAID, which may cause severe stomach bleeding.

The chance is higher if you:

Heart attack and stroke warning
NSAIDs, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be fatal. The risk is higher if you use more than directed or for longer than directed.

DO NOT USE

ASK A DOCTOR BEFORE USE IF

ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE

WHEN USING THIS PRODUCT

STOP USE AND ASK A DOCTOR IF

IF PREGNANT OR BREAST FEEDING,

ask a health professional before use. It is especially important not to use ibuprofen at 20 weeks or later in pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

KEEP OUT OF REACH OF CHILDREN

In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

DIRECTIONS

Other Information

INACTIVE INGREDIENTS

colloidal silicon dioxide, iron oxide red, maize starch, poly ethylene glycol, povidone k-30, pregelatinized starch, sodium starch glycolate, stearic acid, talc, titanium dioxide

QUESTIONS OR COMMENTS?

Call 1-877-770-3183:
weekdays 9:00 AM to 4:30 PM EST

Manufactured By:
Granules India Limited
Hyderabad – 500 043, India
MADE IN INDIA

M.L.No: 37/RR/AP/2003/F/R

Distributed By:
Granules USA, Inc.
Parsippany, NJ 07054

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


NDC# 62207-366-46

See New Warnings Information


ibu-366-250ct-carton.jpg

IBUPROFEN TABLETS USP, 200 mg

Pain Reliever/Fever Reducer (NSAID)*

Contains no ingredient made from a
gluten-containing grain (wheat, barley, or rye)

Do not use if foil inner seal is broken or missing.

250 Coated Caplets

Capsule-Shaped Tablets

Important: Read all product information before using.

Do not use if the foil inner seal is broken or missing

NDC# 62207-366-47

Do not use if the foil inner seal is broken or missing
See New Warnings Information

ibu-366-500ct-label.jpg

IBUPROFEN TABLETS USP, 200 mg

Pain Reliever/Fever Reducer (NSAID)*

Contains no ingredient made from a
gluten-containing grain (wheat, barley, or rye)

Do not use if foil inner seal is broken or missing.

500 Coated Caplets†

†Capsule-Shaped Tablets

Important: Read all product information before using.


NDC# 62207-396-46

See New Warnings Information


ibu-396-250ct-carton.jpgIBUPROFEN TABLETS USP, 200 mg


Pain Reliever/Fever Reducer (NSAID)*

Contains no ingredient made from a
gluten-containing grain (wheat, barley, or rye)

Do not use if foil inner seal is broken or missing.

250 Coated Caplets†

†Capsule-Shaped Tablets

Important: Read all product information before using.



NDC# 62207-396-46

Do not use if the foil inner seal is broken or missing

See New Warnings Information
ibu-396-250ct-label.jpg

IBUPROFEN TABLETS USP, 200 mg

Pain Reliever/Fever Reducer (NSAID)*

Contains no ingredient made from a
gluten-containing grain (wheat, barley, or rye)

Do not use if foil inner seal is broken or missing.

500 Coated Caplets†

†Capsule-Shaped Tablets

Important: Read all product information before using.

IBUPROFEN 
ibuprofen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62207-365
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
Inactive Ingredients
Ingredient NameStrength
STARCH, CORN (UNII: O8232NY3SJ)  
POVIDONE K30 (UNII: U725QWY32X)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
TALC (UNII: 7SEV7J4R1U)  
POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95)  
Product Characteristics
Colorred (Reddish Brown) Scoreno score
ShapeROUNDSize10mm
FlavorImprint Code G;2
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62207-365-5110 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
2NDC:62207-365-4124 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
3NDC:62207-365-4250 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
4NDC:62207-365-43100 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
5NDC:62207-365-46250 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
6NDC:62207-365-47500 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
7NDC:62207-365-48750 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
8NDC:62207-365-491000 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07917401/01/2011
IBUPROFEN 
ibuprofen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62207-366
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
Inactive Ingredients
Ingredient NameStrength
POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95)  
STARCH, CORN (UNII: O8232NY3SJ)  
POVIDONE K30 (UNII: U725QWY32X)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
Colorred (Reddish Brown) Scoreno score
ShapeOVAL ((Capsule shaped tablet)) Size14mm
FlavorImprint Code G;2
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62207-366-5110 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
2NDC:62207-366-4124 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
3NDC:62207-366-4250 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
4NDC:62207-366-43100 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
5NDC:62207-366-46250 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
6NDC:62207-366-47500 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
7NDC:62207-366-48750 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
8NDC:62207-366-491000 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07917401/01/2011
IBUPROFEN 
ibuprofen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62207-396
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
Inactive Ingredients
Ingredient NameStrength
STARCH, CORN (UNII: O8232NY3SJ)  
POVIDONE K30 (UNII: U725QWY32X)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
Colorred (Reddish Brown) Scoreno score
ShapeOVAL ((Capsule shaped tablet)) Size14mm
FlavorImprint Code G;2
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62207-396-5110 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
2NDC:62207-396-4124 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
3NDC:62207-396-4250 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
4NDC:62207-396-43100 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
5NDC:62207-396-46250 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
6NDC:62207-396-47500 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
7NDC:62207-396-48750 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
8NDC:62207-396-491000 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07917408/13/2019
IBUPROFEN 
ibuprofen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62207-395
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
Inactive Ingredients
Ingredient NameStrength
STARCH, CORN (UNII: O8232NY3SJ)  
POVIDONE K30 (UNII: U725QWY32X)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
TALC (UNII: 7SEV7J4R1U)  
POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95)  
Product Characteristics
Colorred (Reddish Brown) Scoreno score
ShapeROUNDSize10mm
FlavorImprint Code G;2
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62207-395-5110 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
2NDC:62207-395-4124 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
3NDC:62207-395-4250 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
4NDC:62207-395-43100 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
5NDC:62207-395-46250 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
6NDC:62207-395-47500 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
7NDC:62207-395-48750 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
8NDC:62207-395-491000 in 1 BOTTLE; Type 0: Not a Combination Product08/13/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07917408/13/2019
Labeler - Granules India Limited (915000087)
Registrant - Granules India Limited (915000087)
Establishment
NameAddressID/FEIBusiness Operations
Granules India Limited918609236manufacture(62207-365, 62207-366, 62207-395, 62207-396)

Revised: 1/2023
Document Id: f37b04a6-8c5f-0644-e053-2995a90a40a0
Set id: fd01353d-1d1d-42b5-9a03-575052189bf5
Version: 18
Effective Time: 20230130
 
Granules India Limited