NDC11 63479070301

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
63479-0703-01	63479-0703
63479-0703-1	63479-0703
63479-703-01	63479-703

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
G03 TEST-MET	ADENOSINE TRIPHOSPHATE, AMMONIUM CHLORIDE, APIS MELLIFERA, BAPTISIA TINCTORIA ROOT, CALCIUM FLUORIDE, CAMPHOR (NATURAL), CITRULLUS COLOCYNTHIS FRUIT PULP, SEQUOIA SEMPERVIRENS BARK, SPONGIA OFFICINALIS SKELETON, ROASTED, TESTOSTERONE	Apex Energetics Inc.	bcbabd20-1941-3f11-e053-2a95a90a06dc	2024-01-08	Warnings	Exact identifier ndc (package): 63479-0703-1 ndc (product): 63479-0703 ndc11 (package): 63479070301

Reported adverse events (FAERS/openFDA)#

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