Class III ยท Low risk
Digoxin Tablets
Cross Contamination with Other Products:(mycophenolate mofetil).
National Drug Code
Is NDC 70954-0201-20 recalled?
Digoxin · 1000 TABLET in 1 BOTTLE (70954-201-20)
Yes — this exact package was recalled
1 FDA recall names the code 70954-0201-20 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
- Digoxin
- Strength
- DIGOXIN .125 mg/1
- Form
- Tablet · Oral
- Labeler
- ANI Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 70954-0201
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
- 70954-0001 See recall 2
- 70954-0002 See recall 2
- 70954-0200 Digoxin 1
- 70954-0531 Estradiol 1
- 70954-0912 Hydroxyzine Hydrochloride 1
Free recall alerts
Know the day your medication is recalled
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