ramipril

Generic: ramipril

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ramipril
Generic Name ramipril
Labeler hikma pharmaceuticals usa inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

ramipril 5 mg/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0054-0108
Product ID 0054-0108_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)
angiotensin converting enzyme inhibitor [epc]
Mechanism of Action
angiotensin-converting enzyme inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00540108
Hyphenated Format 0054-0108

Supplemental Identifiers

RxCUI
198188 198189 261962 845488
UPC
0300540107253 0300540106256 0300540109257 0300540108250
UNII
L35JN3I7SJ
NUI
N0000175562 N0000000181

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 CARTON (0054-0108-20) / 10 CAPSULE in 1 BLISTER PACK
  • 100 CAPSULE in 1 BOTTLE (0054-0108-25)
  • 500 CAPSULE in 1 BOTTLE (0054-0108-29)
source: ndc

Packages (3)

0054-0108-20 10 BLISTER PACK in 1 CARTON (0054-0108-20) / 10 CAPSULE in 1 BLISTER PACK 0054-0108-25 100 CAPSULE in 1 BOTTLE (0054-0108-25) 0054-0108-29 500 CAPSULE in 1 BOTTLE (0054-0108-29)

Ingredients (1)

ramipril (5 mg/1)

Linked Drug Pages (1)

Ramipril ndc-match (0.9)

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": "10 BLISTER PACK in 1 CARTON (0054-0108-20)  / 10 CAPSULE in 1 BLISTER PACK", "package_ndc": "0054-0108-20", "marketing_start_date": "20080618"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0054-0108-25)", "package_ndc": "0054-0108-25", "marketing_start_date": "20080618"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (0054-0108-29)", "package_ndc": "0054-0108-29", "marketing_start_date": "20080618"}], "brand_name": "Ramipril", "product_id": "0054-0108_4019e596-dfb9-43a4-b027-a2bdf6d0f5b4", "dosage_form": "CAPSULE", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "0054-0108", "generic_name": "Ramipril", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ramipril", "active_ingredients": [{"name": "RAMIPRIL", "strength": "5 mg/1"}], "application_number": "ANDA077900", "marketing_category": "ANDA", "marketing_start_date": "20080618", "listing_expiration_date": "20261231"}