NDC11 27808004901

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
27808-0049-01	27808-0049
27808-0049-1	27808-0049
27808-049-01	27808-049

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hydrocodone Bitartrate and Acetaminophen	HYDROCODONE BITARTRATE AND ACETAMINOPHEN	Cranbury Pharmaceuticals, LLC	57e1fe79-eb60-4f4f-bb38-6df0270d408f	2026-01-08	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 27808-049-01 ndc (product): 27808-049 ndc11 (package): 27808004901

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.