FDA.reportPublic FDA data

Ramipril

Product NDC
68788-7198
11-digit product format
687887198
Labeler code
68788
Product ID
68788-7198_22bbd2e8-7436-42c8-8d56-5c55b6630ca9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ramipril
Dosage form
CAPSULE
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA091604
Marketing category
ANDA
Marketing start
2018-07-19
Marketing end
0000-00-00
Substance
RAMIPRIL
Active strength
10 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-7198-1EA - Each68788-71984334bca7-1c94-4e8e-ab4b-9786917f55c912018-09-05
68788-7198-2EA - Each68788-7198352070f2-0460-4c70-af1f-09a1aab5df4712018-09-05
68788-7198-3EA - Each68788-71983ef8be4e-954a-41a4-8697-0b860748f95b12018-09-05
68788-7198-6EA - Each68788-7198764cdee1-a3b0-430e-9ad8-21ffb0e1988412018-09-05
68788-7198-9EA - Each68788-71984704d365-24d4-481f-a963-3aafdf9a495812018-09-05