meloxicam

Generic: meloxicam

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name meloxicam
Generic Name meloxicam
Labeler asclemed usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meloxicam 7.5 mg/1

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-325
Product ID 76420-325_34232f88-5219-6451-e063-6294a90a4469
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077929
Listing Expiration 2026-12-31
Marketing Start 2006-07-19

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420325
Hyphenated Format 76420-325

Supplemental Identifiers

RxCUI
152695 311486
UNII
VG2QF83CGL
NUI
N0000000160 M0001335 N0000175722

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 meloxicam (source: ndc)
Generic Name meloxicam (source: ndc)
Application Number ANDA077929 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 7.5 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (76420-325-00)
  • 100 TABLET in 1 BOTTLE (76420-325-01)
  • 500 TABLET in 1 BOTTLE (76420-325-05)
  • 20 TABLET in 1 BOTTLE (76420-325-20)
  • 30 TABLET in 1 BOTTLE (76420-325-30)
  • 60 TABLET in 1 BOTTLE (76420-325-60)
  • 90 TABLET in 1 BOTTLE (76420-325-90)
source: ndc

Packages (7)

76420-325-00 1000 TABLET in 1 BOTTLE (76420-325-00) 76420-325-01 100 TABLET in 1 BOTTLE (76420-325-01) 76420-325-05 500 TABLET in 1 BOTTLE (76420-325-05) 76420-325-20 20 TABLET in 1 BOTTLE (76420-325-20) 76420-325-30 30 TABLET in 1 BOTTLE (76420-325-30) 76420-325-60 60 TABLET in 1 BOTTLE (76420-325-60) 76420-325-90 90 TABLET in 1 BOTTLE (76420-325-90)

Ingredients (1)

meloxicam (7.5 mg/1)

Linked Drug Pages (1)

MELOXICAM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "34232f88-5219-6451-e063-6294a90a4469", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["VG2QF83CGL"], "rxcui": ["152695", "311486"], "spl_set_id": ["6d7ede5a-c12e-4979-a47a-f3346ea5bc80"], "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": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (76420-325-00)", "package_ndc": "76420-325-00", "marketing_start_date": "20250502"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-325-01)", "package_ndc": "76420-325-01", "marketing_start_date": "20250502"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (76420-325-05)", "package_ndc": "76420-325-05", "marketing_start_date": "20250502"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (76420-325-20)", "package_ndc": "76420-325-20", "marketing_start_date": "20250502"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-325-30)", "package_ndc": "76420-325-30", "marketing_start_date": "20250502"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-325-60)", "package_ndc": "76420-325-60", "marketing_start_date": "20250502"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-325-90)", "package_ndc": "76420-325-90", "marketing_start_date": "20250502"}], "brand_name": "MELOXICAM", "product_id": "76420-325_34232f88-5219-6451-e063-6294a90a4469", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "76420-325", "generic_name": "meloxicam", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MELOXICAM", "active_ingredients": [{"name": "MELOXICAM", "strength": "7.5 mg/1"}], "application_number": "ANDA077929", "marketing_category": "ANDA", "marketing_start_date": "20060719", "listing_expiration_date": "20261231"}