NDC 51655-091

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: 51655-091_e561a5af-c541-4ef0-b027-9d1af884ac72
• NDC: 51655-091
• Product Type: Human Prescription Drug
• Proprietary Name: Levothyroxine
• Generic Name: Levothyroxine
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2014-07-10
• Marketing Category: NDA / NDA
• Application Number: NDA021342
• Labeler Name: Northwind Pharmaceuticals, LLC
• Substance Name: LEVOTHYROXINE SODIUM
• Active Ingredient Strength: 25 ug/1
• Pharm Classes: l-Thyroxine [EPC],Thyroxine [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 51655-091-52

30 TABLET in 1 BOTTLE, DISPENSING (51655-091-52)

• Marketing Start Date: 2014-07-10
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51655-091-52 [51655009152]

Levothyroxine TABLET

• Marketing Category: NDA
• Application Number: NDA021342
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2014-07-10
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
LEVOTHYROXINE SODIUM	25 ug/1

OpenFDA Data

• SPL SET ID: 3177aea1-c0c6-4ae1-b20e-3ca66a949e2c
• Manufacturer:
  • Northwind Pharmaceuticals, LLC
• UNII:
  • 9J765S329G
• RxNorm Concept Unique ID - RxCUI:
  • 966220

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