NAPROXEN- naproxen sodium tablet 
Bryant Ranch Prepack

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gc 951-954L

Active ingredient (in each tablet)

Naproxen sodium 220 mg
(Naproxen 200 mg) (NSAID)*

*nonsteroidal anti-inflammatory drug

Purpose

Pain reliever/ fever reducer

Uses

temporarily relieves minor aches and pain due to:

temporarily reduces fever

Warnings

Allergy alert: Naproxen sodium 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

When using this product

Stop use and ask doctor if

 leg swelling  chest pain
 slurred speech  trouble breathing
 weakness in one part or side of body

If pregnant or breast-feeding, ask a health professional
before use. It is especially important not to use naproxen
sodium during the last 3 months of 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

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

Directions

Storage

Other information

Inactive ingredients

croscarmellose sodium, FD&C blue #2 aluminum lake, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl
alcohol, povidone, silicon dioxide, talc, titanium dioxide

Questions or comments?

Call 1-800-540-3765

HOW SUPPLIED

NDC: 71335-1282-1: 20 Tablets in a BOTTLE

NDC: 71335-1282-2: 30 Tablets in a BOTTLE

NDC: 71335-1282-3: 40 Tablets in a BOTTLE

NDC: 71335-1282-4: 50 Tablets in a BOTTLE

NDC: 71335-1282-5: 60 Tablets in a BOTTLE

NDC: 71335-1282-6: 14 Tablets in a BOTTLE

NDC: 71335-1282-7: 100 Tablets in a BOTTLE

NDC: 71335-1282-8: 90 Tablets in a BOTTLE

NDC: 71335-1282-9: 24 Tablets in a BOTTLE

Naproxen Sodium 220mg Tablet

Label
NAPROXEN 
naproxen sodium tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71335-1282(NDC:57896-954)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NAPROXEN SODIUM (UNII: 9TN87S3A3C) (NAPROXEN - UNII:57Y76R9ATQ) NAPROXEN SODIUM220 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
ColorblueScoreno score
ShapeROUNDSize10mm
FlavorImprint Code 44;417
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71335-1282-120 in 1 BOTTLE; Type 0: Not a Combination Product02/23/2022
2NDC:71335-1282-230 in 1 BOTTLE; Type 0: Not a Combination Product02/23/2022
3NDC:71335-1282-340 in 1 BOTTLE; Type 0: Not a Combination Product02/23/2022
4NDC:71335-1282-450 in 1 BOTTLE; Type 0: Not a Combination Product02/23/2022
5NDC:71335-1282-560 in 1 BOTTLE; Type 0: Not a Combination Product02/23/2022
6NDC:71335-1282-614 in 1 BOTTLE; Type 0: Not a Combination Product02/23/2022
7NDC:71335-1282-7100 in 1 BOTTLE; Type 0: Not a Combination Product02/23/2022
8NDC:71335-1282-890 in 1 BOTTLE; Type 0: Not a Combination Product02/23/2022
9NDC:71335-1282-924 in 1 BOTTLE; Type 0: Not a Combination Product02/23/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20487201/01/2019
Labeler - Bryant Ranch Prepack (171714327)
Registrant - Bryant Ranch Prepack (171714327)
Establishment
NameAddressID/FEIBusiness Operations
Bryant Ranch Prepack171714327REPACK(71335-1282) , RELABEL(71335-1282)

Revised: 3/2023
Document Id: b442a77f-fc48-4f18-841a-a3e4418e2f34
Set id: f9ddc614-26b7-48dc-ae93-02da6388f2d5
Version: 101
Effective Time: 20230330
 
Bryant Ranch Prepack