United States · FDA National Drug Code directory

foster and thrive all day pain relief

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
70677-1137_dc44c5b8-4549-4bbf-871d-5c84d1d97f81
Product NDC
70677-1137
Form
TABLET, FILM COATED
Composition / generic term
Naproxen Sodium
Labeler
Strategic Sourcing Services LLC
Marketing category
ANDA
Marketing start / end (source format)
20230914
Source listing expiry
20261231

Source-listed ingredients

  • NAPROXEN SODIUM — 220 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (70677-1137-1) / 50 TABLET, FILM COATED in 1 BOTTLE · 70677-1137-1
  • 1 BOTTLE in 1 CARTON (70677-1137-2) / 90 TABLET, FILM COATED in 1 BOTTLE · 70677-1137-2

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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