topcare all day pain relief

Generic: naproxen sodium

Labeler: topco associates llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name topcare all day pain relief
Generic Name naproxen sodium
Labeler topco associates llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Topco Associates LLC

Identifiers & Regulatory

Product NDC 36800-368
Product ID 36800-368_526325f7-8883-4c20-802c-544f75249168
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA074661
Listing Expiration 2026-12-31
Marketing Start 1997-01-14

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 36800368
Hyphenated Format 36800-368

Supplemental Identifiers

RxCUI
849574
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 topcare all day pain relief (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA074661 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (36800-368-62) / 24 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (36800-368-71) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (36800-368-75) / 90 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (36800-368-76) / 120 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (36800-368-82) / 200 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (5)

36800-368-62 1 BOTTLE in 1 CARTON (36800-368-62) / 24 TABLET, FILM COATED in 1 BOTTLE 36800-368-71 1 BOTTLE in 1 CARTON (36800-368-71) / 50 TABLET, FILM COATED in 1 BOTTLE 36800-368-75 1 BOTTLE in 1 CARTON (36800-368-75) / 90 TABLET, FILM COATED in 1 BOTTLE 36800-368-76 1 BOTTLE in 1 CARTON (36800-368-76) / 120 TABLET, FILM COATED in 1 BOTTLE 36800-368-82 1 BOTTLE in 1 CARTON (36800-368-82) / 200 TABLET, FILM COATED in 1 BOTTLE

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

TopCare All Day Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "526325f7-8883-4c20-802c-544f75249168", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["079eccdd-33bd-4b5c-bf46-9aef78559082"], "manufacturer_name": ["Topco Associates LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (36800-368-62)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "36800-368-62", "marketing_start_date": "19970722"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (36800-368-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "36800-368-71", "marketing_start_date": "19970114"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (36800-368-75)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "36800-368-75", "marketing_start_date": "20220712"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (36800-368-76)  / 120 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "36800-368-76", "marketing_start_date": "20070629"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (36800-368-82)  / 200 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "36800-368-82", "marketing_start_date": "20040127"}], "brand_name": "TopCare All Day Pain Relief", "product_id": "36800-368_526325f7-8883-4c20-802c-544f75249168", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "36800-368", "generic_name": "Naproxen Sodium", "labeler_name": "Topco Associates LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TopCare All Day Pain Relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "19970114", "listing_expiration_date": "20261231"}