NDC 67877-739 – Ibuprofen
Ibuprofen 800 mg/1 · Tablet, Film Coated · Oral
Product NDC67877-739
Product details
- Brand name
- Ibuprofen
- Generic name
- Ibuprofen
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA214699
- Marketed since
- September 15, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Ibuprofen 800 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 67877-739-01 | 100 TABLET, FILM COATED in 1 BOTTLE (67877-739-01) | Sep 15, 2026 |
| 67877-739-05 | 500 TABLET, FILM COATED in 1 BOTTLE (67877-739-05) | Sep 15, 2026 |
| 67877-739-30 | 30 TABLET, FILM COATED in 1 BOTTLE (67877-739-30) | Sep 15, 2026 |
| 67877-739-33 | 1 BLISTER PACK in 1 CARTON (67877-739-33) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Sep 15, 2026 |
| 67877-739-50 | 50 TABLET, FILM COATED in 1 BOTTLE (67877-739-50) | Sep 15, 2026 |
| 67877-739-60 | 60 TABLET, FILM COATED in 1 BOTTLE (67877-739-60) | Sep 15, 2026 |
| 67877-739-90 | 90 TABLET, FILM COATED in 1 BOTTLE (67877-739-90) | Sep 15, 2026 |
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