captopril

Generic: captopril

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name captopril
Generic Name captopril
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

captopril 12.5 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7105
Product ID 0904-7105_02aa221e-fac5-4dd6-9830-132d4e4f7815
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212809
Listing Expiration 2027-12-31
Marketing Start 2019-12-13

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 09047105
Hyphenated Format 0904-7105

Supplemental Identifiers

RxCUI
308963 317173
UNII
9G64RSX1XD
NUI
N0000175562 N0000000181

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 captopril (source: ndc)
Generic Name captopril (source: ndc)
Application Number ANDA212809 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-7105-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0904-7105-61 100 BLISTER PACK in 1 CARTON (0904-7105-61) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

captopril (12.5 mg/1)

Linked Drug Pages (1)

Captopril ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "02aa221e-fac5-4dd6-9830-132d4e4f7815", "openfda": {"nui": ["N0000175562", "N0000000181"], "unii": ["9G64RSX1XD"], "rxcui": ["308963", "317173"], "spl_set_id": ["a43a5373-ded9-4912-8c98-edaec8352836"], "pharm_class_epc": ["Angiotensin Converting Enzyme Inhibitor [EPC]"], "pharm_class_moa": ["Angiotensin-converting Enzyme Inhibitors [MoA]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7105-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7105-61", "marketing_start_date": "20191213"}], "brand_name": "Captopril", "product_id": "0904-7105_02aa221e-fac5-4dd6-9830-132d4e4f7815", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "0904-7105", "generic_name": "Captopril", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Captopril", "active_ingredients": [{"name": "CAPTOPRIL", "strength": "12.5 mg/1"}], "application_number": "ANDA212809", "marketing_category": "ANDA", "marketing_start_date": "20191213", "listing_expiration_date": "20271231"}