Ramipril

Product NDC
55700-551
11-digit product format
557000551
Labeler code
55700
Product ID
55700-551_b9b07d50-055c-4528-a85d-8abfc11f03ea
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ramipril
Dosage form
CAPSULE
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA077626
Marketing category
ANDA
Marketing start
2017-08-18
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
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-551-30EA - Each55700-55172ee27a7-e88d-45d7-b094-0f10e759c75512018-08-13
55700-551-90EA - Each55700-55183938f1d-86cb-4766-bac5-7d1a8cce580112017-09-11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55700-551-305570005513030 CAPSULE in 1 BOTTLE (55700-551-30) 30 capsule2018-07-060000-00-00NoNoCurrent