fenoprofen calcium
Generic: fenoprofen calcium
Labeler: atland pharmaceuticals, llcDrug Facts
Product Profile
Brand Name
fenoprofen calcium
Generic Name
fenoprofen calcium
Labeler
atland pharmaceuticals, llc
Dosage Form
CAPSULE
Routes
Active Ingredients
fenoprofen calcium 400 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71993-308
Product ID
71993-308_14a4aa5b-30ff-8ad7-e063-6294a90a889e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214475
Listing Expiration
2026-12-31
Marketing Start
2024-03-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71993308
Hyphenated Format
71993-308
Supplemental Identifiers
RxCUI
UPC
UNII
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
fenoprofen calcium (source: ndc)
Generic Name
fenoprofen calcium (source: ndc)
Application Number
ANDA214475 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 400 mg/1
Packaging
- 90 CAPSULE in 1 BOTTLE (71993-308-90)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "14a4aa5b-30ff-8ad7-e063-6294a90a889e", "openfda": {"upc": ["0371993308900"], "unii": ["0X2CW1QABJ"], "rxcui": ["858116"], "spl_set_id": ["3daa336f-2acf-4109-a360-b1d30b192d41"], "manufacturer_name": ["Atland Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71993-308-90)", "package_ndc": "71993-308-90", "marketing_start_date": "20240326"}], "brand_name": "FENOPROFEN CALCIUM", "product_id": "71993-308_14a4aa5b-30ff-8ad7-e063-6294a90a889e", "dosage_form": "CAPSULE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71993-308", "generic_name": "FENOPROFEN CALCIUM", "labeler_name": "Atland Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FENOPROFEN CALCIUM", "active_ingredients": [{"name": "FENOPROFEN CALCIUM", "strength": "400 mg/1"}], "application_number": "ANDA214475", "marketing_category": "ANDA", "marketing_start_date": "20240326", "listing_expiration_date": "20261231"}