captopril

Generic: captopril

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name captopril
Generic Name captopril
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

captopril 50 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-143
Product ID 31722-143_99fac9d2-a1a4-40c3-8530-098acc7e16c6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074737
Listing Expiration 2026-12-31
Marketing Start 2005-12-07

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 31722143
Hyphenated Format 31722-143

Supplemental Identifiers

RxCUI
308962 308963 308964 317173
UPC
0331722144018 0331722143103 0331722141109 0331722141017 0331722142106 0331722142014
UNII
9G64RSX1XD
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 captopril (source: ndc)
Generic Name captopril (source: ndc)
Application Number ANDA074737 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (31722-143-01)
  • 1000 TABLET in 1 BOTTLE (31722-143-10)
source: ndc

Packages (2)

31722-143-01 100 TABLET in 1 BOTTLE (31722-143-01) 31722-143-10 1000 TABLET in 1 BOTTLE (31722-143-10)

Ingredients (1)

captopril (50 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": "99fac9d2-a1a4-40c3-8530-098acc7e16c6", "openfda": {"nui": ["N0000175562", "N0000000181"], "upc": ["0331722144018", "0331722143103", "0331722141109", "0331722141017", "0331722142106", "0331722142014"], "unii": ["9G64RSX1XD"], "rxcui": ["308962", "308963", "308964", "317173"], "spl_set_id": ["5b44ab6e-6cd9-4e12-b9be-d2e4d954acb5"], "pharm_class_epc": ["Angiotensin Converting Enzyme Inhibitor [EPC]"], "pharm_class_moa": ["Angiotensin-converting Enzyme Inhibitors [MoA]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-143-01)", "package_ndc": "31722-143-01", "marketing_start_date": "20210708"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (31722-143-10)", "package_ndc": "31722-143-10", "marketing_start_date": "20210708"}], "brand_name": "Captopril", "product_id": "31722-143_99fac9d2-a1a4-40c3-8530-098acc7e16c6", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "31722-143", "generic_name": "Captopril", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Captopril", "active_ingredients": [{"name": "CAPTOPRIL", "strength": "50 mg/1"}], "application_number": "ANDA074737", "marketing_category": "ANDA", "marketing_start_date": "20051207", "listing_expiration_date": "20261231"}