NDC 68151-1521

Etidronate Disodium

Etidronate Disodium

Etidronate Disodium is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Carilion Materials Management. The primary component is Etidronate Disodium.

• Product ID: 68151-1521_ba1caadc-97b9-4353-b728-7a5cb9ecbe3d
• NDC: 68151-1521
• Product Type: Human Prescription Drug
• Proprietary Name: Etidronate Disodium
• Generic Name: Etidronate Disodium
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2008-01-02
• Marketing Category: ANDA / ANDA
• Application Number: ANDA075800
• Labeler Name: Carilion Materials Management
• Substance Name: ETIDRONATE DISODIUM
• Active Ingredient Strength: 200 mg/1
• Pharm Classes: Bisphosphonate [EPC],Diphosphonates [CS]
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 68151-1521-9

1 TABLET in 1 PACKAGE (68151-1521-9)

• Marketing Start Date: 2008-01-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68151-1521-9 [68151152109]

Etidronate Disodium TABLET

• Marketing Category: ANDA
• Application Number: ANDA075800
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2008-01-02
• Marketing End Date: 2019-12-31

Drug Details

Active Ingredients

Ingredient	Strength
ETIDRONATE DISODIUM	200 mg/1

OpenFDA Data

• SPL SET ID: dcbd076e-3989-4cae-9466-54a0e9118128
• Manufacturer:
  • Carilion Materials Management
• UNII:
  • M16PXG993G
• RxNorm Concept Unique ID - RxCUI:
  • 904535

Pharmacological Class

• Bisphosphonate [EPC]
• Diphosphonates [CS]

NDC Crossover Matching brand name "Etidronate Disodium" or generic name "Etidronate Disodium"

NDC	Brand Name	Generic Name
0378-3286	Etidronate Disodium	etidronate disodium
0378-3288	Etidronate Disodium	etidronate disodium
68151-1521	Etidronate Disodium	etidronate disodium