FDA.reportPublic FDA data

Phentermine hydrochloride

Product NDC
51655-877
11-digit product format
516550877
Labeler code
51655
Product ID
51655-877_04e78751-69ff-4966-9af2-5ac4f21837fa
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Phentermine hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Northwind Pharmaceuticals
Application
ANDA040555
Marketing category
ANDA
Marketing start
2014-06-01
Marketing end
0000-00-00
Substance
PHENTERMINE HYDROCHLORIDE
Active strength
38 mg/1
Pharmacologic classes
Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]
DEA schedule
CIV
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
51655-877-522026-01-08C16284748780-19d75b9d1-2292-f424-e053-dadaa90a57ceef39df14-1a3e-4eff-8285-2c113ce2d291
51655-877-902026-01-08C16284748780-19d75b9d1-2292-f424-e053-dadaa90a57ceef39df14-1a3e-4eff-8285-2c113ce2d291
51655-877-522020-01-31C16284748780-19d75b9d1-2292-f424-e053-dadaa90a57ceef39df14-1a3e-4eff-8285-2c113ce2d291
51655-877-902020-01-31C16284748780-19d75b9d1-2292-f424-e053-dadaa90a57ceef39df14-1a3e-4eff-8285-2c113ce2d291

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PHENTERMINE HYDROCHLORIDEACTIVE INGREDIENT0K2I505OTVPHENTERMINE HYDROCHLORIDE TABLET [NORTHWIND PHARMACEUTICALS]1
PHENTERMINEACTIVE MOIETYC045TQL4WPPHENTERMINE HYDROCHLORIDE TABLET [NORTHWIND PHARMACEUTICALS]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-877PHENTERMINE HYDROCHLORIDE TABLET [NORTHWIND PHARMACEUTICALS]1Legacy NDC20140619_ef39df14-1a3e-4eff-8285-2c113ce2d291.zip