NDC 59762-5000

Sulfasalazine

Sulfasalazine

Sulfasalazine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Greenstone Llc. The primary component is Sulfasalazine.

• Product ID: 59762-5000_052d6e84-a2f0-4526-b8c0-61d84b3b1863
• NDC: 59762-5000
• Product Type: Human Prescription Drug
• Proprietary Name: Sulfasalazine
• Generic Name: Sulfasalazine
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2003-07-01
• Marketing Category: NDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC
• Application Number: NDA007073
• Labeler Name: Greenstone LLC
• Substance Name: SULFASALAZINE
• Active Ingredient Strength: 500 mg/1
• Pharm Classes: Aminosalicylate [EPC],Aminosalicylic Acids [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 59762-5000-1

100 TABLET in 1 BOTTLE (59762-5000-1)

• Marketing Start Date: 2003-07-01
• Marketing End Date: 2024-11-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 59762-5000-1 [59762500001]

Sulfasalazine TABLET

• Marketing Category: NDA AUTHORIZED GENERIC
• Application Number: NDA007073
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2003-07-01

NDC 59762-5000-2 [59762500002]

Sulfasalazine TABLET

• Marketing Category: NDA AUTHORIZED GENERIC
• Application Number: NDA007073
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2016-05-26

NDC 59762-5000-5 [59762500005]

Sulfasalazine TABLET

• Marketing Category: NDA AUTHORIZED GENERIC
• Application Number: NDA007073
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2020-04-13

NDC 59762-5000-6 [59762500006]

Sulfasalazine TABLET

• Marketing Category: NDA AUTHORIZED GENERIC
• Application Number: NDA007073
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2020-04-13

Drug Details

Active Ingredients

Ingredient	Strength
SULFASALAZINE	500 mg/1

OpenFDA Data

• SPL SET ID: 48fbc535-a33a-45ee-85ff-9d1ec9b31d9c
• Manufacturer:
  • Greenstone LLC
• UNII:
  • 3XC8GUZ6CB
• RxNorm Concept Unique ID - RxCUI:
  • 198232
• UPC Code:
  • 0359762500014

Pharmacological Class

• Aminosalicylate [EPC]
• Aminosalicylic Acids [CS]

Medicade Reported Pricing

59762500002 SULFASALAZINE 500 MG TABLET

Pricing Unit: EA | Drug Type:

59762500001 SULFASALAZINE 500 MG TABLET

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "Sulfasalazine" or generic name "Sulfasalazine"

NDC	Brand Name	Generic Name
0093-3234	Sulfasalazine	Sulfasalazine
0591-0796	Sulfasalazine	Sulfasalazine
0603-5801	Sulfasalazine	sulfasalazine
10544-288	Sulfasalazine	sulfasalazine
23155-019	Sulfasalazine	Sulfasalazine
33261-756	Sulfasalazine	sulfasalazine
43353-495	Sulfasalazine	Sulfasalazine
50090-0086	Sulfasalazine	Sulfasalazine
50090-2013	Sulfasalazine	Sulfasalazine
50268-730	Sulfasalazine	Sulfasalazine
59762-0104	Sulfasalazine	Sulfasalazine
68071-4215	Sulfasalazine	Sulfasalazine
68788-9021	SULFASALAZINE	SULFASALAZINE
70518-0185	Sulfasalazine	Sulfasalazine
70518-1829	Sulfasalazine	Sulfasalazine
59762-5000	Sulfasalazine	Sulfasalazine
63629-5688	Sulfasalazine	Sulfasalazine
70518-2342	Sulfasalazine	Sulfasalazine
0013-0101	Azulfidine	Sulfasalazine
0013-0102	Azulfidine	Sulfasalazine