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NDC 51655-0275-20 IBUPROFEN 800 mg/1 Details

IBUPROFEN 800 mg/1

IBUPROFEN is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals. The primary component is IBUPROFEN.

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: 51655-0275-20
Last Updated: 04/21/2024
MedLinePlus Full Drug Details: Ibuprofen

Product Information

NDC	51655-0275
Product ID	51655-275_d9f2ae7d-6c41-6429-e053-2a95a90ab8dc
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
Proprietary Name Suffix	n/a
Non-Proprietary Name	IBUPROFEN
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	800
Active Ingredient Units	mg/1
Substance Name	IBUPROFEN
Labeler Name	Northwind Pharmaceuticals
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	ANDA090796
Listing Certified Through	2024-12-31

Package

NDC 51655-0275-20 (51655027520)

Pricing Information	N/A
NDC Package Code	51655-275-20
Billing NDC	51655027520
Package	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-20)
Marketing Start Date	2021-07-09
NDC Exclude Flag	N