tolmetin sodium
Generic: tolmetin sodium
Labeler: rising pharma holdings, inc.Drug Facts
Product Profile
Brand Name
tolmetin sodium
Generic Name
tolmetin sodium
Labeler
rising pharma holdings, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
tolmetin sodium 400 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
16571-826
Product ID
16571-826_a6175635-172e-4b9e-8388-b60c2aa117a2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA073393
Marketing Start
2023-06-30
Marketing End
2026-05-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
16571826
Hyphenated Format
16571-826
Supplemental Identifiers
RxCUI
UPC
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
tolmetin sodium (source: ndc)
Generic Name
tolmetin sodium (source: ndc)
Application Number
ANDA073393 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 400 mg/1
Packaging
- 90 CAPSULE in 1 BOTTLE (16571-826-09)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a6175635-172e-4b9e-8388-b60c2aa117a2", "openfda": {"upc": ["0316571826094"], "unii": ["02N1TZF99F"], "rxcui": ["198296"], "spl_set_id": ["740a0f37-aa95-4558-b415-be516b8c40a3"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (16571-826-09)", "package_ndc": "16571-826-09", "marketing_end_date": "20260531", "marketing_start_date": "20230630"}], "brand_name": "Tolmetin Sodium", "product_id": "16571-826_a6175635-172e-4b9e-8388-b60c2aa117a2", "dosage_form": "CAPSULE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "16571-826", "generic_name": "Tolmetin Sodium", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tolmetin Sodium", "active_ingredients": [{"name": "TOLMETIN SODIUM", "strength": "400 mg/1"}], "application_number": "ANDA073393", "marketing_category": "ANDA", "marketing_end_date": "20260531", "marketing_start_date": "20230630"}