NDC 55111-396 – Famotidine
Famotidine 20 mg/1 · Tablet · Oral
Product NDC55111-396
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Dr.Reddys Laboratories Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077367
- Marketed since
- September 30, 2006
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 55111-396-01 | 1 BOTTLE in 1 CARTON (55111-396-01) / 100 TABLET in 1 BOTTLE | Sep 30, 2006 |
| 55111-396-08 | 1 BLISTER PACK in 1 CARTON (55111-396-08) / 8 TABLET in 1 BLISTER PACK | Sep 30, 2006 |
| 55111-396-13 | 1 BOTTLE in 1 CARTON (55111-396-13) / 130 TABLET in 1 BOTTLE | Oct 1, 2020 |
| 55111-396-16 | 5 BLISTER PACK in 1 CARTON (55111-396-16) / 5 TABLET in 1 BLISTER PACK | Sep 30, 2006 |
| 55111-396-32 | 1 BOTTLE in 1 CARTON (55111-396-32) / 170 TABLET in 1 BOTTLE | Sep 30, 2006 |
| 55111-396-35 | 1 BOTTLE in 1 CARTON (55111-396-35) / 25 TABLET in 1 BOTTLE | Sep 30, 2006 |
| 55111-396-44 | 2 BOTTLE in 1 CARTON (55111-396-44) / 100 TABLET in 1 BOTTLE | Sep 30, 2006 |
| 55111-396-50 | 1 BOTTLE in 1 CARTON (55111-396-50) / 50 TABLET in 1 BOTTLE | Sep 30, 2006 |
| 55111-396-65 | 1 BOTTLE in 1 CARTON (55111-396-65) / 65 TABLET in 1 BOTTLE | Oct 1, 2020 |
| 55111-396-90 | 1 BOTTLE in 1 CARTON (55111-396-90) / 90 TABLET in 1 BOTTLE | Oct 7, 2021 |
Recalls mentioning this NDC
- D-0009-2018 Oct 18, 2017 · Class III
Failed impurities/degradation specifications: Famotodine has an out of specification result for an individual related substance observed during routine stability testing of a batch for related…
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