NDC 67877-626 – Ibuprofen and famotidine
Ibuprofen 800 mg/1; Famotidine 26.6 mg/1 · Tablet, Film Coated · Oral
Product NDC67877-626
Product details
- Brand name
- Ibuprofen and famotidine
- Generic name
- Ibuprofen and famotidine
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA211890
- Marketed since
- August 4, 2021
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-2 Receptor Antagonist; Nonsteroidal Anti-inflammatory Drug
Active ingredients
- Ibuprofen 800 mg/1
- Famotidine 26.6 mg/1
Uses, dosage, side effects and warnings for Ibuprofen And Famotidine →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 67877-626-01 | 100 TABLET, FILM COATED in 1 BOTTLE (67877-626-01) | Aug 4, 2021 |
| 67877-626-05 | 500 TABLET, FILM COATED in 1 BOTTLE (67877-626-05) | Aug 4, 2021 |
| 67877-626-06 | 6 BLISTER PACK in 1 CARTON (67877-626-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK | Aug 4, 2021 |
| 67877-626-90 | 90 TABLET, FILM COATED in 1 BOTTLE (67877-626-90) | Aug 4, 2021 |
Recalls mentioning this NDC
- D-0237-2024 Jan 24, 2024 · Class II
Presence of Foreign Tablet/Capsule: A stray Rasagiline Mesylate 1 mg tablet was discovered in an unopened bottle of Ibuprofen and Famotidine.
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