NDC 51655-005

Phendimetrazine

Phendimetrazine

Phendimetrazine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Northwind Pharmaceuticals. The primary component is Phendimetrazine Tartrate.

• Product ID: 51655-005_4a64fde2-1db8-5878-e054-00144ff8d46c
• NDC: 51655-005
• Product Type: Human Prescription Drug
• Proprietary Name: Phendimetrazine
• Generic Name: Phendimetrazine
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2015-04-22
• Marketing Category: ANDA / ANDA
• Application Number: ANDA091042
• Labeler Name: Northwind Pharmaceuticals
• Substance Name: PHENDIMETRAZINE TARTRATE
• Active Ingredient Strength: 35 mg/1
• Pharm Classes: Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]
• DEA Schedule: CIII
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 51655-005-52

30 TABLET in 1 BOTTLE (51655-005-52)

• Marketing Start Date: 2015-04-22
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51655-005-52 [51655000552]

Phendimetrazine TABLET

• Marketing Category: ANDA
• Application Number: ANDA091042
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2015-04-22

Drug Details

Active Ingredients

Ingredient	Strength
PHENDIMETRAZINE TARTRATE	35 mg/1

OpenFDA Data

• SPL SET ID: 4a64fde2-1db7-5878-e054-00144ff8d46c
• Manufacturer:
  • Northwind Pharmaceuticals
• UNII:
  • 6985IP0T80
• RxNorm Concept Unique ID - RxCUI:
  • 979549

Pharmacological Class

• Appetite Suppression [PE]
• Increased Sympathetic Activity [PE]
• Sympathomimetic Amine Anorectic [EPC]