relafen ds
Generic: nabumetone
Labeler: carwin pharmaceutical associates, llcDrug Facts
Product Profile
Brand Name
relafen ds
Generic Name
nabumetone
Labeler
carwin pharmaceutical associates, llc
Dosage Form
TABLET
Routes
Active Ingredients
nabumetone 1000 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
15370-170
Product ID
15370-170_48aa3640-1dd2-4693-9b0d-a99595b97a0e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203166
Listing Expiration
2026-12-31
Marketing Start
2019-09-20
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
15370170
Hyphenated Format
15370-170
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
relafen ds (source: ndc)
Generic Name
nabumetone (source: ndc)
Application Number
ANDA203166 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1000 mg/1
Packaging
- 100 TABLET in 1 BOTTLE, PLASTIC (15370-170-10)
- 30 TABLET in 1 BOTTLE, PLASTIC (15370-170-30)
- 60 TABLET in 1 BOTTLE, PLASTIC (15370-170-60)
- 1 BLISTER PACK in 1 CARTON (15370-170-99) / 2 TABLET in 1 BLISTER PACK
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48aa3640-1dd2-4693-9b0d-a99595b97a0e", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0315370170308"], "unii": ["LW0TIW155Z"], "rxcui": ["427726", "2200291"], "spl_set_id": ["a9a0af85-6c43-4a2d-ba75-0be4ca64c931"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Carwin Pharmaceutical Associates, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (15370-170-10)", "package_ndc": "15370-170-10", "marketing_start_date": "20220512"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (15370-170-30)", "package_ndc": "15370-170-30", "marketing_start_date": "20190920"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (15370-170-60)", "package_ndc": "15370-170-60", "marketing_start_date": "20200228"}, {"sample": true, "description": "1 BLISTER PACK in 1 CARTON (15370-170-99) / 2 TABLET in 1 BLISTER PACK", "package_ndc": "15370-170-99", "marketing_start_date": "20200228"}], "brand_name": "RELAFEN DS", "product_id": "15370-170_48aa3640-1dd2-4693-9b0d-a99595b97a0e", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "15370-170", "generic_name": "NABUMETONE", "labeler_name": "Carwin Pharmaceutical Associates, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RELAFEN DS", "active_ingredients": [{"name": "NABUMETONE", "strength": "1000 mg/1"}], "application_number": "ANDA203166", "marketing_category": "ANDA", "marketing_start_date": "20190920", "listing_expiration_date": "20261231"}