NDC 65862-859 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-859
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA206530
- Marketed since
- December 22, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 65862-859-01 | 100 TABLET, FILM COATED in 1 BOTTLE (65862-859-01) | Dec 22, 2015 |
| 65862-859-05 | 500 TABLET, FILM COATED in 1 BOTTLE (65862-859-05) | Dec 22, 2015 |
| 65862-859-30 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-859-30) | Dec 22, 2015 |
| 65862-859-78 | 10 BLISTER PACK in 1 CARTON (65862-859-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-859-10) | Dec 22, 2015 |
| 65862-859-99 | 1000 TABLET, FILM COATED in 1 BOTTLE (65862-859-99) | Dec 22, 2015 |
Recalls mentioning this NDC
- D-0290-2021 Mar 10, 2021 · Class II
Presence of foreign tablets/capsules: Famotidine 20mg and ibuprofen 400mg tablets were found in a lot of famotidine 40mg.
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