United States · FDA National Drug Code directory

IBUPROFEN

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
59556-764_7d889b12-7d30-423f-a988-bb1d201ebb59
Product NDC
59556-764
Form
CAPSULE, LIQUID FILLED
Composition / generic term
IBUPROFEN
Labeler
Strides Pharma Inc
Marketing category
ANDA
Marketing start / end (source format)
20221116
Source listing expiry
20271231

Source-listed ingredients

  • IBUPROFEN — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (59556-764-11) / 120 CAPSULE, LIQUID FILLED in 1 BOTTLE · 59556-764-11
  • 1 BOTTLE in 1 CARTON (59556-764-12) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE · 59556-764-12
  • 1 BOTTLE in 1 CARTON (59556-764-13) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE · 59556-764-13
  • 1 BOTTLE in 1 CARTON (59556-764-18) / 180 CAPSULE, LIQUID FILLED in 1 BOTTLE · 59556-764-18
  • 1 BOTTLE in 1 CARTON (59556-764-29) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE · 59556-764-29
  • 1 BOTTLE in 1 CARTON (59556-764-48) / 160 CAPSULE, LIQUID FILLED in 1 BOTTLE · 59556-764-48
  • 1 BOTTLE in 1 CARTON (59556-764-49) / 200 CAPSULE, LIQUID FILLED in 1 BOTTLE · 59556-764-49
  • 1 BOTTLE in 1 CARTON (59556-764-50) / 300 CAPSULE, LIQUID FILLED in 1 BOTTLE · 59556-764-50
  • 3000 CAPSULE, LIQUID FILLED in 1 BAG (59556-764-92) · 59556-764-92

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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