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VARIVAX
VARIVAX - 0006-4826-00 - (Varicella Virus Vaccine Live)
Drug Information of VARIVAX
| Product NDC: | 0006-4826 |
| Proprietary Name: | VARIVAX |
| Non Proprietary Name: | Varicella Virus Vaccine Live |
| Active Ingredient(s): | 1350 [PFU]/.5mL & nbsp; Varicella Virus Vaccine Live |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of VARIVAX
| Product NDC: | 0006-4826 |
| Labeler Name: | Merck Sharp & Dohme Corp. |
| Product Type: | VACCINE |
| FDA Application Number: | BLA103552 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19950317 |
Package Information of VARIVAX
| Package NDC: | 0006-4826-00 |
| Package Description: | 1 VIAL, SINGLE-DOSE in 1 CARTON (0006-4826-00) > .5 mL in 1 VIAL, SINGLE-DOSE (0006-4826-01) |
NDC Information of VARIVAX
| NDC Code | 0006-4826-00 |
| Proprietary Name | VARIVAX |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (0006-4826-00) > .5 mL in 1 VIAL, SINGLE-DOSE (0006-4826-01) |
| Product NDC | 0006-4826 |
| Product Type Name | VACCINE |
| Non Proprietary Name | Varicella Virus Vaccine Live |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 19950317 |
| Marketing Category Name | BLA |
| Labeler Name | Merck Sharp & Dohme Corp. |
| Substance Name | VARICELLA-ZOSTER VIRUS STRAIN OKA/MERCK LIVE ANTIGEN |
| Strength Number | 1350 |
| Strength Unit | [PFU]/.5mL |
| Pharmaceutical Classes | Live Attenuated Varicella Zoster Virus Vaccine [EPC],Actively Acquired Immunity [PE],Vaccines, Attenuated [Chemical/Ingredient],Chickenpox Vaccine [Chemical/Ingredient],Live Attenuated Herpes Zoster Virus Vaccine [EPC],Herpes Zoster Vaccine [Chemical/Ingredient] |
