NDC11 70700010185

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
70700-0101-85	70700-0101
70700-101-85	70700-101

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
Norethindrone Acetate and Ethinyl Estradiol	NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL TABLETS AND FERROUS FUMARATE TABLETS	Xiromed, LLC	b4bc4302-9484-465a-090d-47e1e0360b73	2023-07-12	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 70700-101-85 ndc (product): 70700-101 ndc11 (package): 70700010185

Reported adverse events (FAERS/openFDA)#

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