NDC11 00009470913

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
00009-4709-13	00009-4709
0009-4709-13	0009-4709

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
Depo-SubQ Provera	MEDROXYPROGESTERONE ACETATE	Pharmacia & Upjohn Company LLC	390087a6-f3c3-4f0b-a930-79acf412f153	2025-12-18	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 0009-4709-13 ndc (product): 0009-4709 ndc11 (package): 00009470913

Reported adverse events (FAERS/openFDA)#

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