NDC 0378-2150

Meclofenamate Sodium

Meclofenamate Sodium

Meclofenamate Sodium is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Mylan Pharmaceuticals Inc.. The primary component is Meclofenamate Sodium.

• Product ID: 0378-2150_03f3ded6-0711-49f1-986b-b9a60f1f3cb7
• NDC: 0378-2150
• Product Type: Human Prescription Drug
• Proprietary Name: Meclofenamate Sodium
• Generic Name: Meclofenamate Sodium
• Dosage Form: Capsule
• Route of Administration: ORAL
• Marketing Start Date: 1986-09-03
• Marketing Category: ANDA / ANDA
• Application Number: ANDA071081
• Labeler Name: Mylan Pharmaceuticals Inc.
• Substance Name: MECLOFENAMATE SODIUM
• Active Ingredient Strength: 50 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0378-2150-01

100 CAPSULE in 1 BOTTLE, PLASTIC (0378-2150-01)

• Marketing Start Date: 1986-09-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0378-2150-01 [00378215001]

Meclofenamate Sodium CAPSULE

• Marketing Category: ANDA
• Application Number: ANDA071081
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1986-09-03

Drug Details

Active Ingredients

Ingredient	Strength
MECLOFENAMATE SODIUM	50 mg/1

OpenFDA Data

• SPL SET ID: 96f19af4-de8f-4fd7-90d8-55fe6ebdd81d
• Manufacturer:
  • Mylan Pharmaceuticals Inc.
• UNII:
  • 94NJ818U2W
• RxNorm Concept Unique ID - RxCUI:
  • 618552
  • 618557

NDC Crossover Matching brand name "Meclofenamate Sodium" or generic name "Meclofenamate Sodium"

NDC	Brand Name	Generic Name
0378-2150	Meclofenamate Sodium	meclofenamate sodium
0378-3000	Meclofenamate Sodium	meclofenamate sodium