NDC 51672-2130 – Ibuprofen
Ibuprofen 100 mg/5mL · Suspension · Oral
Product NDC51672-2130
Product details
- Brand name
- Ibuprofen
- Generic name
- Ibuprofen
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Suspension
- Route
- Oral
- Marketing category
- ANDA · ANDA209207
- Marketed since
- June 27, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Ibuprofen 100 mg/5mL
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51672-2130-1 | 1 BOTTLE in 1 CARTON (51672-2130-1) / 240 mL in 1 BOTTLE | Jun 27, 2017 |
| 51672-2130-8 | 1 BOTTLE in 1 CARTON (51672-2130-8) / 120 mL in 1 BOTTLE | Jun 27, 2017 |
Recalls mentioning this NDC
- D-0300-2020 Nov 6, 2019 · Class II
Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small particles of an inert plastic material introduced during manufacturing. - D-0301-2020 Nov 6, 2019 · Class II
Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small particles of an inert plastic material introduced during manufacturing.
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