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
- 17856-5309_34f37e2c-ba78-120a-e063-6294a90aa750
- Product NDC
- 17856-5309
- Form
- SUSPENSION
- Composition / generic term
- Ibuprofen
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19990207
- Source listing expiry
- 20261231
Source-listed ingredients
- IBUPROFEN — 100 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 mL in 1 SYRINGE (17856-5309-1) · 17856-5309-1
- 10 mL in 1 SYRINGE (17856-5309-2) · 17856-5309-2
- 20 mL in 1 CUP (17856-5309-4) · 17856-5309-4
- 5 mL in 1 CUP (17856-5309-5) · 17856-5309-5
- 15 mL in 1 CUP (17856-5309-6) · 17856-5309-6
- 7.5 mL in 1 CUP, UNIT-DOSE (17856-5309-7) · 17856-5309-7
- 72 CUP, UNIT-DOSE in 1 CASE (17856-5309-8) / 10 mL in 1 CUP, UNIT-DOSE · 17856-5309-8
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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