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NDC 70518-2342-00 Sulfasalazine 500 mg/1 Details

Sulfasalazine 500 mg/1

Sulfasalazine is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is SULFASALAZINE.

MedlinePlus Drug Summary

Sulfasalazine is used to treat ulcerative colitis (a condition which causes swelling and sores in the lining of the colon [large intestine] and rectum) and also to maintain improvement of ulcerative colitis symptoms. Sulfasalazine delayed-release (Azulfidine EN-tabs) is also used to treat rheumatoid arthritis in adults whose disease has not responded well to other medications or could not be tolerated. Sulfasalazine delayed-release (Azulfidine EN-tabs) is also used to treat polyarticular juvenile idiopathic arthritis (PJIA; a type of childhood arthritis that affects five or more joints during the first six months of the condition, causing pain, swelling, and loss of function) in children who have not been helped by other medications. Sulfasalazine is in a class of medications called anti-inflammatory drugs. It works by reducing inflammation (swelling) inside the body.

Related Packages: 70518-2342-00
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Sulfasalazine

Product Information

NDC	70518-2342
Product ID	70518-2342_039b8b45-79ac-65c8-e063-6394a90a2b86
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	Sulfasalazine
Proprietary Name Suffix	n/a
Non-Proprietary Name	Sulfasalazine
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	500
Active Ingredient Units	mg/1
Substance Name	SULFASALAZINE
Labeler Name	REMEDYREPACK INC.
Pharmaceutical Class	Aminosalicylate [EPC], Aminosalicylic Acids [CS]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA085828
Listing Certified Through	n/a

Package

NDC 70518-2342-00 (70518234200)

Pricing Information	N/A
NDC Package Code	70518-2342-0
Billing NDC	70518234200
Package	270 TABLET in 1 BOTTLE, PLASTIC (70518-2342-0)
Marketing Start Date	2019-10-03
NDC Exclude Flag	N