tolmetin sodium

Generic: tolmetin sodium

Labeler: atland pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tolmetin sodium
Generic Name tolmetin sodium
Labeler atland pharmaceuticals, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

tolmetin sodium 600 mg/1

Manufacturer
Atland Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 71993-312
Product ID 71993-312_24ffd8d5-f836-4914-b4d9-1cc420e01fa3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074473
Listing Expiration 2026-12-31
Marketing Start 2025-02-25

Pharmacologic Class

Classes
anti-inflammatory agents non-steroidal [cs] cyclooxygenase inhibitors [moa] nonsteroidal anti-inflammatory drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71993312
Hyphenated Format 71993-312

Supplemental Identifiers

RxCUI
198297
UPC
0371993312303
UNII
02N1TZF99F

Packaging Origin

Original Packager
true

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 ANDA074473 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71993-312-30)
source: ndc

Packages (1)

71993-312-30 30 TABLET, FILM COATED in 1 BOTTLE (71993-312-30)

Ingredients (1)

tolmetin sodium (600 mg/1)

Linked Drug Pages (1)

Tolmetin Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "24ffd8d5-f836-4914-b4d9-1cc420e01fa3", "openfda": {"upc": ["0371993312303"], "unii": ["02N1TZF99F"], "rxcui": ["198297"], "spl_set_id": ["e6150446-c5ef-4437-b488-067876649fcc"], "manufacturer_name": ["Atland Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71993-312-30)", "package_ndc": "71993-312-30", "marketing_start_date": "20250225"}], "brand_name": "Tolmetin Sodium", "product_id": "71993-312_24ffd8d5-f836-4914-b4d9-1cc420e01fa3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71993-312", "generic_name": "Tolmetin Sodium", "labeler_name": "Atland Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tolmetin Sodium", "active_ingredients": [{"name": "TOLMETIN SODIUM", "strength": "600 mg/1"}], "application_number": "ANDA074473", "marketing_category": "ANDA", "marketing_start_date": "20250225", "listing_expiration_date": "20261231"}