Altace - 49999-871-90 - (Ramipril)

Alphabetical Index


Drug Information of Altace

Product NDC: 49999-871
Proprietary Name: Altace
Non Proprietary Name: Ramipril
Active Ingredient(s): 10    mg/1 & nbsp;   Ramipril
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Altace

Product NDC: 49999-871
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019901
Marketing Category: NDA
Start Marketing Date: 20100524

Package Information of Altace

Package NDC: 49999-871-90
Package Description: 90 CAPSULE in 1 BOTTLE, PLASTIC (49999-871-90)

NDC Information of Altace

NDC Code 49999-871-90
Proprietary Name Altace
Package Description 90 CAPSULE in 1 BOTTLE, PLASTIC (49999-871-90)
Product NDC 49999-871
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ramipril
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100524
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name RAMIPRIL
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Altace


General Information