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NDC 00363-0909-49 Ibuprofen Sodium 256 mg/1 Details
Ibuprofen Sodium 256 mg/1
Ibuprofen Sodium is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreen Company. The primary component is IBUPROFEN SODIUM.
MedlinePlus Drug Summary
Prescription ibuprofen is used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints) and rheumatoid arthritis (arthritis caused by swelling of the lining of the joints). It is also used to relieve mild to moderate pain, including menstrual pain (pain that happens before or during a menstrual period). Nonprescription ibuprofen is used to reduce fever and to relieve minor aches and pain from headaches, muscle aches, arthritis, menstrual periods, the common cold, toothaches, and backaches. Ibuprofen is in a class of medications called NSAIDs. It works by stopping the body's production of a substance that causes pain, fever, and inflammation.
Related Packages: 00363-0909-49Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Ibuprofen
Product Information
| NDC | 00363-0909 |
|---|---|
| Product ID | 0363-0909_5dada37e-65d3-40b4-83ff-dbfc316e9f45 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Ibuprofen Sodium |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Ibuprofen |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 256 |
| Active Ingredient Units | mg/1 |
| Substance Name | IBUPROFEN SODIUM |
| Labeler Name | Walgreen Company |
| Pharmaceutical Class | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA206581 |
| Listing Certified Through | 2023-12-31 |
Package
Package Images
NDC 00363-0909-49 (00363090949)
| NDC Package Code | 0363-0909-49 |
|---|---|
| Billing NDC | 00363090949 |
| Package | 1 BOTTLE in 1 CARTON (0363-0909-49) / 40 TABLET, FILM COATED in 1 BOTTLE |
| Marketing Start Date | 2016-01-13 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL f2a30365-b3dd-4360-8998-e5277d4d17b7 Details
Active ingredient (in each tablet)
Uses
Warnings
Allergy alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin.
Symptoms may include:
- •
- hives
- •
- facial swelling
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- asthma (wheezing)
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- shock
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- skin reddening
- •
- rash
- •
- blisters
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:
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- are age 60 or older
- •
- have had stomach ulcers or bleeding problems
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- take a blood thinning (anticoagulant) or steroid drug
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- take other drugs containing prescription or nonprescription NSAIDs [aspirin, ibuprofen, naproxen, or others]
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- have 3 or more alcoholic drinks every day while using this product
- •
- take more or for a longer time than directed
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
- •
- stomach bleeding warning applies to you
- •
- you have problems or serious side effects from taking pain relievers or fever reducers
- •
- you have a history of stomach problems, such as heartburn
- •
- you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma or had a stroke
- •
- you are taking a diuretic
Ask a doctor or pharmacist before use if you are
Stop use and ask a doctor if
- •
- you experience any of the following signs of stomach bleeding:
- •
- feel faint
- •
- vomit blood
- •
- have bloody or black stools
- •
- have stomach pain that does not get better
- •
- you have symptoms of heart problems or stroke:
- •
- chest pain
- •
- trouble breathing
- •
- weakness in one part or side of body
- •
- slurred speech
- •
- leg swelling
- •
- pain gets worse or lasts more than 10 days
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- fever gets worse or lasts more than 3 days
- •
- redness or swelling is present in the painful area
- •
- any new symptoms appear
If pregnant or breast-feeding,
Keep out of reach of children.
Directions
- •
- do not take more than directed
- •
- the smallest effective dose should be used
- •
- adults and children 12 years and over: take 1 tablet every 4 to 6 hours while symptoms persist
- •
- if pain or fever does not respond to 1 tablet, 2 tablets may be used
- •
- do not exceed 6 tablets in 24 hours, unless directed by a doctor
- •
- children under 12 years: ask a doctor
Other information
Inactive ingredients
Package/Label Principal Display Panel
INGREDIENTS AND APPEARANCE
| IBUPROFEN SODIUM
ibuprofen tablet, film coated |
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| Labeler - Walgreen Company (008965063) |