FDA.reportPublic FDA data

Doxycycline Hyclate

Product NDC
51655-184
11-digit product format
516550184
Labeler code
51655
Product ID
51655-184_05a17f94-218e-49aa-9d33-6a0d832f40b2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Doxycycline Hyclate
Dosage form
TABLET
Route
ORAL
Labeler
Northwind Pharmaceuticals
Application
ANDA062031
Marketing category
ANDA
Marketing start
2014-09-15
Marketing end
0000-00-00
Substance
DOXYCYCLINE HYCLATE
Active strength
100 mg/1
Pharmacologic classes
Tetracycline-class Drug [EPC],Tetracyclines [CS]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51655-184-202026-01-08C16284748780-19d75b9cf-e1c8-f424-e053-dadaa90a57ceb333a1c0-1b70-4061-8a47-bca045f0cf28
51655-184-202020-01-31C16284748780-19d75b9cf-e1c8-f424-e053-dadaa90a57ceb333a1c0-1b70-4061-8a47-bca045f0cf28

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DOXYCYCLINE HYCLATEACTIVE INGREDIENT19XTS3T51UDOXYCYCLINE HYCLATE TABLET [NORTHWIND PHARMACEUTICALS]1
DOXYCYCLINE ANHYDROUSACTIVE MOIETY334895S862DOXYCYCLINE HYCLATE TABLET [NORTHWIND PHARMACEUTICALS]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-184DOXYCYCLINE HYCLATE TABLET [NORTHWIND PHARMACEUTICALS]1Legacy NDC20141030_b333a1c0-1b70-4061-8a47-bca045f0cf28.zip