Ramipril

Product NDC
70518-4607
11-digit product format
705184607
Labeler code
70518
Product ID
70518-4607_5020e36d-6732-bf08-e063-6294a90a0c9b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ramipril
Dosage form
CAPSULE
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA091604
Marketing category
ANDA
Marketing start
2026-04-22
Substance
RAMIPRIL
Active strength
5 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Ramipril
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
RAMIPRIL5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL35JN3I7SJ
Rxcui198189

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9a7d2f1c-330a-4830-b88b-315f5c1bab6bProduct name120151208
c76eceed-99b6-9572-9f36-9ac63b4b3ce4Product name220141218

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-4607-0Ramipril50 in 1 BOXCAPSULE501
70518-4607-1Ramipril1 in 1 POUCHCAPSULE11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198189ramipril 5 MG Oral CapsulePSNfcf42121-8e85-4eae-82b4-bc029653b4621
198189ramipril 5 MG Oral CapsuleSCDfcf42121-8e85-4eae-82b4-bc029653b4621

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
70518-4607-07051846070050 POUCH in 1 BOX (70518-4607-0) / 1 CAPSULE in 1 POUCH (70518-4607-1) 50 pouch2026-04-22NoNoHistorical
70518-4607-1705184607011 in 1 POUCHHistorical