Class II ยท Moderate risk
Acyclovir Tablets
Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir Tablets USP 400 mg actually contained Carvedilol Tablets 6.25 mg
National Drug Code
Is NDC 68382-0791-01 recalled?
acyclovir · 100 TABLET in 1 BOTTLE (68382-791-01)
Yes — this exact package was recalled
1 FDA recall names the code 68382-0791-01 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
- acyclovir
- Strength
- ACYCLOVIR 400 mg/1
- Form
- Tablet · Oral
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Type
- Human Prescription Drug
- Product code
- 68382-0791
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
- 68382-0021 Venlafaxine 2
- 68382-0033 See recall 2
- 68382-0095 Carvedilol 2
- 68382-0099 Paroxetine 2
- 68382-0110 Bromocriptine mesylate 2
- 68382-0123 Amlodipine Besylate 2
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