Home NDC 58160-828 NDC 58160-828 - Shingrix This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 58160-828
Package NDCs from labels 58160-828-03, 58160-828-01
Manufacturer GlaxoSmithKline Biologicals SA
Effective date 2026-02-13
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58160-828-03 Shingrix 0.5 mL in 1 VIAL INJECTION, POWDER, LYOPHILIZED, 5 mL 50 ug in 0.5mL 23 58160-828-03 Shingrix 0.5 mL in 1 VIAL INJECTION, POWDER, LYOPHILIZED, 10 mL 50 ug in 0.5mL 6 58160-828-01 Shingrix 0.5 mL in 1 VIAL INJECTION, POWDER, LYOPHILIZED, 1 mL 50 ug in 0.5mL 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58160-828 SHINGRIX (ZOSTER VACCINE RECOMBINANT, ADJUVANTED) KIT [GLAXOSMITHKLINE BIOLOGICALS SA] 19 Unmatched 20250327_0280849d-5c78-4a9d-8941-4eab429f6bd8.zip 58160-828 SHINGRIX (ZOSTER VACCINE RECOMBINANT, ADJUVANTED) KIT [A-S MEDICATION SOLUTIONS] 6 Unmatched 20240110_279a251c-f4d0-4c47-b999-7ef1a45ac0d0.zip 58160-828 SHINGRIX (ZOSTER VACCINE RECOMBINANT, ADJUVANTED) KIT [A-S MEDICATION SOLUTIONS] 2 Unmatched 20210416_e9ba0102-8cbb-4c4c-810e-292119095a8a.zip