Details for New Drug Application (NDA): 074885
NDA 074885 describes ACYCLOVIR IN SODIUM CHLORIDE 0.9% PRESERVATIVE FREE, which is a drug marketed by Eurohlth Intl Sarl and is included in one NDA. Additional details are available on the ACYCLOVIR IN SODIUM CHLORIDE 0.9% PRESERVATIVE FREE profile page.
The generic ingredient in ACYCLOVIR IN SODIUM CHLORIDE 0.9% PRESERVATIVE FREE is acyclovir sodium. There is one drug master file entry for this compound. Eight suppliers are listed for this compound. Additional details are available on the acyclovir sodium profile page.
The generic ingredient in ACYCLOVIR IN SODIUM CHLORIDE 0.9% PRESERVATIVE FREE is acyclovir sodium. There is one drug master file entry for this compound. Eight suppliers are listed for this compound. Additional details are available on the acyclovir sodium profile page.
Summary for 074885
| Tradename: | ACYCLOVIR IN SODIUM CHLORIDE 0.9% PRESERVATIVE FREE |
| Applicant: | Eurohlth Intl Sarl |
| Ingredient: | acyclovir sodium |
| Patents: | 0 |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE;INJECTION | Strength | EQ 500MG BASE/VIAL | ||||
| Approval Date: | Dec 19, 1997 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE;INJECTION | Strength | EQ 1GM BASE/VIAL | ||||
| Approval Date: | Dec 19, 1997 | TE: | RLD: | No | |||||
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