naproxen sodium

Generic: naproxen sodium

Labeler: kroger company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen sodium
Generic Name naproxen sodium
Labeler kroger company
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Kroger Company

Identifiers & Regulatory

Product NDC 30142-954
Product ID 30142-954_ee849c66-1cf3-2a24-16bf-8b8c36198f07
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075168
Listing Expiration 2026-12-31
Marketing Start 2021-08-04

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 30142954
Hyphenated Format 30142-954

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 naproxen sodium (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA075168 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (30142-954-10) / 100 TABLET, COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (30142-954-20) / 200 TABLET, COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (30142-954-50) / 500 TABLET, COATED in 1 BOTTLE
source: ndc

Packages (3)

30142-954-10 1 BOTTLE in 1 CARTON (30142-954-10) / 100 TABLET, COATED in 1 BOTTLE 30142-954-20 1 BOTTLE in 1 CARTON (30142-954-20) / 200 TABLET, COATED in 1 BOTTLE 30142-954-50 1 BOTTLE in 1 CARTON (30142-954-50) / 500 TABLET, COATED in 1 BOTTLE

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

Naproxen Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ee849c66-1cf3-2a24-16bf-8b8c36198f07", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["30bcf289-0039-f389-73c4-fef3e8861034"], "manufacturer_name": ["Kroger Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-954-10)  / 100 TABLET, COATED in 1 BOTTLE", "package_ndc": "30142-954-10", "marketing_start_date": "20210804"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-954-20)  / 200 TABLET, COATED in 1 BOTTLE", "package_ndc": "30142-954-20", "marketing_start_date": "20210804"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-954-50)  / 500 TABLET, COATED in 1 BOTTLE", "package_ndc": "30142-954-50", "marketing_start_date": "20210804"}], "brand_name": "Naproxen Sodium", "product_id": "30142-954_ee849c66-1cf3-2a24-16bf-8b8c36198f07", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "30142-954", "generic_name": "Naproxen Sodium", "labeler_name": "Kroger Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA075168", "marketing_category": "ANDA", "marketing_start_date": "20210804", "listing_expiration_date": "20261231"}