NDC 72657-113 – Famotidine
Famotidine 20 mg/1 · Tablet, Film Coated · Oral
Product NDC72657-113
Product details
- Brand name
- Famotidine
- Generic name
- Famotidine
- Labeler
- GLENMARK THERAPEUTICS INC., USA
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA215822
- Marketed since
- June 1, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-2 Receptor Antagonist
Active ingredients
- Famotidine 20 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 72657-113-20 | 1 BOTTLE in 1 CARTON (72657-113-20) / 200 TABLET, FILM COATED in 1 BOTTLE | Jun 1, 2022 |
| 72657-113-88 | 1 BOTTLE in 1 CARTON (72657-113-88) / 85 TABLET, FILM COATED in 1 BOTTLE | Jun 1, 2022 |
Recalls mentioning this NDC
- D-0939-2023 Jul 26, 2023 · Class II
Labeling: Label Error on Declared Strength: some cartons labeled and containing 20 mg may have an external label placed on the side of the carton indicating strength as 10 mg.
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