NDC 68382-791 – Acyclovir
Acyclovir 400 mg/1 · Tablet · Oral
Product NDC68382-791
Product details
- Brand name
- Acyclovir
- Generic name
- Acyclovir
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA204314
- Marketed since
- September 10, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor
Active ingredients
- Acyclovir 400 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68382-791-01 | 100 TABLET in 1 BOTTLE (68382-791-01) | Sep 10, 2014 |
| 68382-791-05 | 500 TABLET in 1 BOTTLE (68382-791-05) | Sep 10, 2014 |
| 68382-791-06 | 30 TABLET in 1 BOTTLE (68382-791-06) | Sep 10, 2014 |
| 68382-791-10 | 1000 TABLET in 1 BOTTLE (68382-791-10) | Sep 10, 2014 |
| 68382-791-16 | 90 TABLET in 1 BOTTLE (68382-791-16) | Sep 10, 2014 |
| 68382-791-30 | 10 BLISTER PACK in 1 CARTON (68382-791-30) / 10 TABLET in 1 BLISTER PACK | Sep 10, 2014 |
Recalls mentioning this NDC
- D-1272-2019 May 15, 2019 · Class II
Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir Tablets USP 400 mg actually contained Carvedilol Tablets 6.25 mg
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