Home NDC 49281-561 NDC 49281-561 - PENTACEL 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 49281-561
Package NDCs from labels 49281-561-01
Manufacturer Sanofi Vaccines US Inc. | Sanofi Vaccines Canada Ltd.
Effective date 2026-04-28
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 49281-561-01 PENTACEL 0.5 mL in 1 VIAL, SINGLE-DOSE INJECTION, SUSPENSION 2.5 mL 26 [D'ag'U] in 0.5mL 13 49281-561-01 PENTACEL 0.5 mL in 1 VIAL, SINGLE-DOSE INJECTION, SUSPENSION 2.5 mL 7 [D'ag'U] in 0.5mL 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49281-561 PENTACEL (DIPHTHERIA AND TETANUS TOXOIDS AND ACELLULAR PERTUSSIS ADSORBED, INACTIVATED POLIOVIRUS AND HAEMOPHILUS B CONJUGATE (TETANUS TOXOID CONJUGATE) VACCINE) KIT [SANOFI PASTEUR INC.] 9 Unmatched 20250403_67d5c665-ca88-49ba-b7d3-7145d9878cf0.zip 49281-561 PENTACEL (DIPHTHERIA AND TETANUS TOXOIDS AND ACELLULAR PERTUSSIS ADSORBED, INACTIVATED POLIOVIRUS AND HAEMOPHILUS B CONJUGATE (TETANUS TOXOID CONJUGATE) VACCINE) KIT [A-S MEDICATION SOLUTIONS] 1 Unmatched 20250523_e7a819d7-a597-4c91-9078-7cd20ac34410.zip