NDC 76420-891 – Ibuprofen and famotidine
Ibuprofen 800 mg/1; Famotidine 26.6 mg/1 · Tablet, Film Coated · Oral
Product NDC76420-891
Product details
- Brand name
- Ibuprofen and famotidine
- Generic name
- Ibuprofen and famotidine
- Labeler
- Asclemed USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA211890
- Marketed since
- August 4, 2021
- Listing expires
- December 31, 2026
- 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 76420-891-01 | 100 TABLET, FILM COATED in 1 BOTTLE (76420-891-01) | Jan 2, 2025 |
| 76420-891-05 | 500 TABLET, FILM COATED in 1 BOTTLE (76420-891-05) | Jan 2, 2025 |
| 76420-891-06 | 6 BLISTER PACK in 1 CARTON (76420-891-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK | Jan 2, 2025 |
| 76420-891-30 | 30 TABLET, FILM COATED in 1 BOTTLE (76420-891-30) | Jan 2, 2025 |
| 76420-891-60 | 60 TABLET, FILM COATED in 1 BOTTLE (76420-891-60) | Jan 2, 2025 |
| 76420-891-90 | 90 TABLET, FILM COATED in 1 BOTTLE (76420-891-90) | Jan 2, 2025 |
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