dipentum
Generic: olsalazine sodium
Labeler: viatris specialty llcDrug Facts
Product Profile
Brand Name
dipentum
Generic Name
olsalazine sodium
Labeler
viatris specialty llc
Dosage Form
CAPSULE, GELATIN COATED
Routes
Active Ingredients
olsalazine sodium 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0037-6860
Product ID
0037-6860_9a4c3abc-74c9-4a2c-a8e3-fc0100d873d9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA019715
Listing Expiration
2026-12-31
Marketing Start
2015-05-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00376860
Hyphenated Format
0037-6860
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
dipentum (source: ndc)
Generic Name
olsalazine sodium (source: ndc)
Application Number
NDA019715 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (0037-6860-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9a4c3abc-74c9-4a2c-a8e3-fc0100d873d9", "openfda": {"unii": ["Y7JEW0XG7I"], "rxcui": ["905162", "905164"], "spl_set_id": ["8512d0c6-db4e-4673-b3b4-28975c18413f"], "manufacturer_name": ["Viatris Specialty LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (0037-6860-10)", "package_ndc": "0037-6860-10", "marketing_start_date": "20150515"}], "brand_name": "Dipentum", "product_id": "0037-6860_9a4c3abc-74c9-4a2c-a8e3-fc0100d873d9", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Aminosalicylate [EPC]", "Aminosalicylic Acids [CS]"], "product_ndc": "0037-6860", "generic_name": "olsalazine sodium", "labeler_name": "Viatris Specialty LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dipentum", "active_ingredients": [{"name": "OLSALAZINE SODIUM", "strength": "250 mg/1"}], "application_number": "NDA019715", "marketing_category": "NDA", "marketing_start_date": "20150515", "listing_expiration_date": "20261231"}