Phentermine hydrochloride

Product NDC: 51655-876
11-digit product format: 516550876
Labeler code: 51655
Product ID: 51655-876_d1d6b361-ba56-4c9d-875b-c4fa75323ccf
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Phentermine hydrochloride
Dosage form: TABLET
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA040377
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
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-876-25	2026-01-08	C162847	48780-1	9d75b9d1-228f-f424-e053-dadaa90a57ce	bcc89055-4996-4bae-b77e-a09f08ed7f28
51655-876-25	2020-01-31	C162847	48780-1	9d75b9d1-228f-f424-e053-dadaa90a57ce	bcc89055-4996-4bae-b77e-a09f08ed7f28

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
PHENTERMINE HYDROCHLORIDE	ACTIVE INGREDIENT	0K2I505OTV	PHENTERMINE HYDROCHLORIDE TABLET [NORTHWIND PHARMACEUTICALS]	1
PHENTERMINE	ACTIVE MOIETY	C045TQL4WP	PHENTERMINE HYDROCHLORIDE TABLET [NORTHWIND PHARMACEUTICALS]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-876	PHENTERMINE HYDROCHLORIDE TABLET [NORTHWIND PHARMACEUTICALS]	1	Legacy NDC	20140619_bcc89055-4996-4bae-b77e-a09f08ed7f28.zip