Ramipril

Product NDC
60687-332
11-digit product format
606870332
Labeler code
60687
Product ID
60687-332_8d2e27e5-304f-b151-e053-2995a90a3f32
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ramipril
Dosage form
CAPSULE
Route
ORAL
Labeler
American Health Packaging
Application
ANDA078832
Marketing category
ANDA
Marketing start
2017-10-13
Marketing end
2019-08-31
Substance
RAMIPRIL
Active strength
3 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60687-332-01EA - Each60687-3328ec3fdca-0773-413f-93ba-40d07d0b96d012017-11-06
60687-332-11EA - Each60687-3324c6e6f5a-a14a-4fb5-b7f4-bd53ede114f512017-11-06