fenoprofen calcium

Generic: fenoprofen calcium

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fenoprofen calcium
Generic Name fenoprofen calcium
Labeler rising pharma holdings, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

fenoprofen calcium 300 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 16571-887
Product ID 16571-887_ba5e0066-40c5-4ea4-bd0c-cfcb18bdbc48
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214475
Listing Expiration 2026-12-31
Marketing Start 2024-07-26

Pharmacologic Class

Classes
anti-inflammatory agents non-steroidal [cs] cyclooxygenase inhibitors [moa] nonsteroidal anti-inflammatory drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16571887
Hyphenated Format 16571-887

Supplemental Identifiers

RxCUI
197694 197695 858116
UPC
0316571688098
UNII
0X2CW1QABJ

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 fenoprofen calcium (source: ndc)
Generic Name fenoprofen calcium (source: ndc)
Application Number ANDA214475 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (16571-887-01)
source: ndc

Packages (1)

16571-887-01 100 CAPSULE in 1 BOTTLE (16571-887-01)

Ingredients (1)

fenoprofen calcium (300 mg/1)

Linked Drug Pages (1)

FENOPROFEN CALCIUM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ba5e0066-40c5-4ea4-bd0c-cfcb18bdbc48", "openfda": {"upc": ["0316571688098"], "unii": ["0X2CW1QABJ"], "rxcui": ["197694", "197695", "858116"], "spl_set_id": ["4aa38cca-9f8f-4ab6-8103-4f1f48801a43"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (16571-887-01)", "package_ndc": "16571-887-01", "marketing_start_date": "20240726"}], "brand_name": "FENOPROFEN CALCIUM", "product_id": "16571-887_ba5e0066-40c5-4ea4-bd0c-cfcb18bdbc48", "dosage_form": "CAPSULE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "16571-887", "generic_name": "FENOPROFEN CALCIUM", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FENOPROFEN CALCIUM", "active_ingredients": [{"name": "FENOPROFEN CALCIUM", "strength": "300 mg/1"}], "application_number": "ANDA214475", "marketing_category": "ANDA", "marketing_start_date": "20240726", "listing_expiration_date": "20261231"}