Class II ยท Moderate risk
Famotidine Tablets
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.
National Drug Code
Is NDC 72657-0113-20 recalled?
Famotidine · 1 BOTTLE in 1 CARTON (72657-113-20) / 200 TABLET, FILM COATED in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 72657-0113-20 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Famotidine
- Strength
- FAMOTIDINE 20 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Glenmark Therapeutics INC., USA
- Type
- Human OTC Drug
- Product code
- 72657-0113
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 72657-0129 Cetirizine HCl 1
- 72657-0157 Acetaminophen, Ibuprofen 1
Free recall alerts
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