NDC 99207-487-10 - Dynacin

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 99207-487
Requested NDC: 99207-487-10
Package NDCs from labels: 99207-487-10, 99207-487-11
Manufacturer: MEDICIS, The Dermatology Company
Effective date: 2006-11-28
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Dynacin - MEDICIS, The Dermatology Company	MEDICIS, The Dermatology Company	2006-11-28	HUMAN PRESCRIPTION DRUG LABELING

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
minocycline hydrochloride	ACTIVE INGREDIENT	0020414E5U	DYNACIN (MINOCYCLINE HYDROCHLORIDE) CAPSULE [MEDICIS, THE DERMATOLOGY COMPANY]	1
minocycline	ACTIVE MOIETY	FYY3R43WGO	DYNACIN (MINOCYCLINE HYDROCHLORIDE) CAPSULE [MEDICIS, THE DERMATOLOGY COMPANY]	1
gelatin	INACTIVE INGREDIENT	2G86QN327L	DYNACIN (MINOCYCLINE HYDROCHLORIDE) CAPSULE [MEDICIS, THE DERMATOLOGY COMPANY]	1
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	DYNACIN (MINOCYCLINE HYDROCHLORIDE) CAPSULE [MEDICIS, THE DERMATOLOGY COMPANY]	1
silicon dioxide	INACTIVE INGREDIENT	ETJ7Z6XBU4	DYNACIN (MINOCYCLINE HYDROCHLORIDE) CAPSULE [MEDICIS, THE DERMATOLOGY COMPANY]	1
sodium lauryl sulfate	INACTIVE INGREDIENT	368GB5141J	DYNACIN (MINOCYCLINE HYDROCHLORIDE) CAPSULE [MEDICIS, THE DERMATOLOGY COMPANY]	1
starch (corn)	INACTIVE INGREDIENT		DYNACIN (MINOCYCLINE HYDROCHLORIDE) CAPSULE [MEDICIS, THE DERMATOLOGY COMPANY]	1
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	DYNACIN (MINOCYCLINE HYDROCHLORIDE) CAPSULE [MEDICIS, THE DERMATOLOGY COMPANY]	1

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
EAC291B8-16D7-6600-0567-B8582030AAA1			42C69D40-E716-4347-9351-F8D8E1E65085	2006-11-28	Warnings, Adverse reactions	Exact identifier spl id: EAC291B8-16D7-6600-0567-B8582030AAA1 spl set id: 42C69D40-E716-4347-9351-F8D8E1E65085

Reported adverse events (FAERS/openFDA)#

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