ramipril
Generic: ramipril
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
ramipril
Generic Name
ramipril
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
ramipril 1.25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0054-0106
Product ID
0054-0106_4019e596-dfb9-43a4-b027-a2bdf6d0f5b4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077900
Listing Expiration
2026-12-31
Marketing Start
2008-06-18
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00540106
Hyphenated Format
0054-0106
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
ramipril (source: ndc)
Generic Name
ramipril (source: ndc)
Application Number
ANDA077900 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1.25 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (0054-0106-25)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4019e596-dfb9-43a4-b027-a2bdf6d0f5b4", "openfda": {"nui": ["N0000175562", "N0000000181"], "upc": ["0300540107253", "0300540106256", "0300540109257", "0300540108250"], "unii": ["L35JN3I7SJ"], "rxcui": ["198188", "198189", "261962", "845488"], "spl_set_id": ["7e9e84f7-ff47-463d-bf47-7a9745960aae"], "pharm_class_epc": ["Angiotensin Converting Enzyme Inhibitor [EPC]"], "pharm_class_moa": ["Angiotensin-converting Enzyme Inhibitors [MoA]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0054-0106-25)", "package_ndc": "0054-0106-25", "marketing_start_date": "20080618"}], "brand_name": "Ramipril", "product_id": "0054-0106_4019e596-dfb9-43a4-b027-a2bdf6d0f5b4", "dosage_form": "CAPSULE", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "0054-0106", "generic_name": "Ramipril", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ramipril", "active_ingredients": [{"name": "RAMIPRIL", "strength": "1.25 mg/1"}], "application_number": "ANDA077900", "marketing_category": "ANDA", "marketing_start_date": "20080618", "listing_expiration_date": "20261231"}