NDC 49708-521

Flumadine

Flumadine

Flumadine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Caraco Pharma, Inc.. The primary component is Rimantadine Hydrochloride.

• Product ID: 49708-521_3f2752c1-89c7-483d-a974-e47b75ffa259
• NDC: 49708-521
• Product Type: Human Prescription Drug
• Proprietary Name: Flumadine
• Generic Name: Flumadine
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2009-09-22
• Marketing Category: NDA / NDA
• Application Number: NDA019649
• Labeler Name: Caraco Pharma, Inc.
• Substance Name: RIMANTADINE HYDROCHLORIDE
• Active Ingredient Strength: 100 mg/1
• Pharm Classes: Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA]
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 49708-521-88

100 TABLET in 1 BOTTLE (49708-521-88)

• Marketing Start Date: 2009-09-22
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 49708-521-88 [49708052188]

Flumadine TABLET

• Marketing Category: NDA
• Application Number: NDA019649
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-09-22
• Marketing End Date: 2017-08-31

Drug Details

Active Ingredients

Ingredient	Strength
RIMANTADINE HYDROCHLORIDE	100 mg/1

Pharmacological Class

• Influenza A M2 Protein Inhibitor [EPC]
• M2 Protein Inhibitors [MoA]