NDC 71335-3121 – Ibuprofen
Ibuprofen 600 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-3121
Product details
- Brand name
- Ibuprofen
- Generic name
- Ibuprofen
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202413
- Marketed since
- May 23, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Ibuprofen 600 mg/1
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-3121-0 | 21 TABLET, FILM COATED in 1 BOTTLE (71335-3121-0) | Apr 13, 2026 |
| 71335-3121-1 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-3121-1) | Apr 13, 2026 |
| 71335-3121-2 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-3121-2) | Apr 13, 2026 |
| 71335-3121-3 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-3121-3) | Apr 13, 2026 |
| 71335-3121-4 | 40 TABLET, FILM COATED in 1 BOTTLE (71335-3121-4) | Apr 13, 2026 |
| 71335-3121-5 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-3121-5) | Apr 13, 2026 |
| 71335-3121-6 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-3121-6) | Apr 13, 2026 |
| 71335-3121-7 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-3121-7) | Apr 13, 2026 |
| 71335-3121-8 | 50 TABLET, FILM COATED in 1 BOTTLE (71335-3121-8) | Apr 13, 2026 |
| 71335-3121-9 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-3121-9) | Apr 13, 2026 |
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