NDC 50268-062 – Acyclovir
Acyclovir 800 mg/1 · Tablet · Oral
Product NDC50268-062
Product details
- Brand name
- Acyclovir
- Generic name
- Acyclovir
- Labeler
- AvPAK
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA075382
- Marketed since
- July 18, 2014
- Listing expires
- December 31, 2027
- 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 800 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 50268-062-15 | 50 BLISTER PACK in 1 BOTTLE, UNIT-DOSE (50268-062-15) / 1 TABLET in 1 BLISTER PACK (50268-062-11) | Jul 18, 2014 |
Recalls mentioning this NDC
- D-0544-2018 Mar 7, 2018 · Class II
Presence of Foreign Tablet/Capsule; cartons labeled to contain Acyclovir tablets may contain Torsemide tablets in some of the blister cavities.
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