NDC11 10202001012

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
10202-0010-12	10202-0010
10202-010-12	10202-010

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
Ultra Strength Antacid Wintergreen Flavor	CALCIUM CARBONATE	7-ELEVEN	2f3c4e78-71d2-c46c-e063-6394a90a210a	2025-02-28	Warnings	Exact identifier ndc (package): 10202-010-12 ndc (product): 10202-010 ndc11 (package): 10202001012

Reported adverse events (FAERS/openFDA)#

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