NDC 55150-154 – Acyclovir Sodium
Acyclovir Sodium 500 mg/10mL · Injection, Solution · Intravenous
Product NDC55150-154
Product details
- Brand name
- Acyclovir Sodium
- Generic name
- Acyclovir Sodium
- Labeler
- Eugia US LLC
- Dosage form
- Injection, Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA203701
- Marketed since
- October 11, 2013
- 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 Sodium 500 mg/10mL
Uses, dosage, side effects and warnings for Acyclovir Sodium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 55150-154-10 | 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-154-10) / 10 mL in 1 VIAL, SINGLE-DOSE | Oct 11, 2013 |
| 55150-154-11 | 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-154-11) / 10 mL in 1 VIAL, SINGLE-DOSE | Oct 11, 2013 |
Recalls mentioning this NDC
- D-0095-2023 Jan 11, 2023 · Class II
Presence of Particulate Matter: Customer complaint of dark particles found inside the vial - D-0013-2023 Oct 26, 2022 · Class II
Presence of Particulate Matter: Customer complaint for a dark red, brown and black particulate floating inside vial.