proxen np 660

Generic: naproxen sodium

Labeler: opmx llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name proxen np 660
Generic Name naproxen sodium
Labeler opmx llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
OPMX LLC

Identifiers & Regulatory

Product NDC 69729-123
Product ID 69729-123_0d811063-82c1-bf9f-e063-6294a90aa371
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA091353
Listing Expiration 2026-12-31
Marketing Start 2023-11-07

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 69729123
Hyphenated Format 69729-123

Supplemental Identifiers

RxCUI
849574
UPC
0810053181362 0810053181379 0810053181423
UNII
9TN87S3A3C

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 proxen np 660 (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA091353 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (69729-123-12) / 12 TABLET in 1 BLISTER PACK
  • 2 BLISTER PACK in 1 CARTON (69729-123-24) / 12 TABLET in 1 BLISTER PACK
  • 50 POUCH in 1 CARTON (69729-123-50) / 2 TABLET in 1 POUCH
source: ndc

Packages (3)

69729-123-12 1 BLISTER PACK in 1 CARTON (69729-123-12) / 12 TABLET in 1 BLISTER PACK 69729-123-24 2 BLISTER PACK in 1 CARTON (69729-123-24) / 12 TABLET in 1 BLISTER PACK 69729-123-50 50 POUCH in 1 CARTON (69729-123-50) / 2 TABLET in 1 POUCH

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

PROXEN NP 660 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0d811063-82c1-bf9f-e063-6294a90aa371", "openfda": {"upc": ["0810053181362", "0810053181379", "0810053181423"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["09990b2f-202e-b4df-e063-6394a90a055b"], "manufacturer_name": ["OPMX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (69729-123-12)  / 12 TABLET in 1 BLISTER PACK", "package_ndc": "69729-123-12", "marketing_start_date": "20231107"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (69729-123-24)  / 12 TABLET in 1 BLISTER PACK", "package_ndc": "69729-123-24", "marketing_start_date": "20231116"}, {"sample": false, "description": "50 POUCH in 1 CARTON (69729-123-50)  / 2 TABLET in 1 POUCH", "package_ndc": "69729-123-50", "marketing_start_date": "20231107"}], "brand_name": "PROXEN NP 660", "product_id": "69729-123_0d811063-82c1-bf9f-e063-6294a90aa371", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69729-123", "generic_name": "Naproxen Sodium", "labeler_name": "OPMX LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PROXEN NP 660", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA091353", "marketing_category": "ANDA", "marketing_start_date": "20231107", "listing_expiration_date": "20261231"}