NDC 51672-5321 – ibuprofen
Ibuprofen 100 mg/5mL · Suspension · Oral
Product NDC51672-5321
Product details
- Brand name
- ibuprofen
- Generic name
- ibuprofen
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Suspension
- Route
- Oral
- Marketing category
- ANDA · ANDA211666
- Marketed since
- August 15, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Ibuprofen 100 mg/5mL
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51672-5321-1 | 1 BOTTLE, PLASTIC in 1 CARTON (51672-5321-1) / 240 mL in 1 BOTTLE, PLASTIC | Oct 10, 2024 |
| 51672-5321-8 | 1 BOTTLE, PLASTIC in 1 CARTON (51672-5321-8) / 120 mL in 1 BOTTLE, PLASTIC | Aug 15, 2024 |
Recalls mentioning this NDC
- D-0390-2026 Mar 25, 2026 · Class II
Presence of foreign substance: the firm received complaints for a gel-like mass and black particles in the product.
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