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
- 62207-366_1f8c5711-4342-d41b-e063-6394a90acb7a
- Product NDC
- 62207-366
- Form
- TABLET
- Composition / generic term
- Ibuprofen
- Labeler
- Granules India Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110101
- Source listing expiry
- 20271231
Source-listed ingredients
- IBUPROFEN — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 24 TABLET in 1 BOTTLE (62207-366-41) · 62207-366-41
- 50 TABLET in 1 BOTTLE (62207-366-42) · 62207-366-42
- 100 TABLET in 1 BOTTLE (62207-366-43) · 62207-366-43
- 250 TABLET in 1 BOTTLE (62207-366-46) · 62207-366-46
- 500 TABLET in 1 BOTTLE (62207-366-47) · 62207-366-47
- 750 TABLET in 1 BOTTLE (62207-366-48) · 62207-366-48
- 1000 TABLET in 1 BOTTLE (62207-366-49) · 62207-366-49
- 10 TABLET in 1 BOTTLE (62207-366-51) · 62207-366-51
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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