NDC 51655-290

LEVOTHYROXINE

Levothyroxine

LEVOTHYROXINE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Northwind Pharmaceuticals, Llc. The primary component is Levothyroxine Sodium.

• Product ID: 51655-290_64f1daf6-af49-4087-a874-974fed3ecb79
• NDC: 51655-290
• Product Type: Human Prescription Drug
• Proprietary Name: LEVOTHYROXINE
• Generic Name: Levothyroxine
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2014-09-14
• Marketing Category: NDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC
• Application Number: NDA021210
• Labeler Name: Northwind Pharmaceuticals, LLC
• Substance Name: LEVOTHYROXINE SODIUM
• Active Ingredient Strength: 125 ug/1
• Pharm Classes: l-Thyroxine [EPC],Thyroxine [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 51655-290-52

30 TABLET in 1 BOTTLE, DISPENSING (51655-290-52)

• Marketing Start Date: 2014-09-14
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51655-290-52 [51655029052]

LEVOTHYROXINE TABLET

• Marketing Category: NDA authorized generic
• Application Number: NDA021210
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-09-14
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
LEVOTHYROXINE SODIUM	125 ug/1

OpenFDA Data

• SPL SET ID: bd1ce5e4-9dd5-4bd5-ae5e-c88822c04f98
• Manufacturer:
  • Northwind Pharmaceuticals, LLC
• UNII:
  • 9J765S329G
• RxNorm Concept Unique ID - RxCUI:
  • 966224

Pharmacological Class

• l-Thyroxine [EPC]
• Thyroxine [CS]

NDC Crossover Matching brand name "LEVOTHYROXINE" or generic name "Levothyroxine"

NDC	Brand Name	Generic Name
43742-0955	Levothyroxine	Levothyroxine
51655-091	Levothyroxine	Levothyroxine
51655-290	LEVOTHYROXINE	LEVOTHYROXINE