naproxen sodium headache pain
Generic: naproxen sodium
Labeler: dr.reddy's laboratories incDrug Facts
Product Profile
Brand Name
naproxen sodium headache pain
Generic Name
naproxen sodium
Labeler
dr.reddy's laboratories inc
Dosage Form
TABLET, COATED
Routes
Active Ingredients
naproxen sodium 220 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43598-071
Product ID
43598-071_c94f5885-67ab-4e95-df53-a58f119c504b
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA075168
Listing Expiration
2026-12-31
Marketing Start
2021-12-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43598071
Hyphenated Format
43598-071
Supplemental Identifiers
RxCUI
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
naproxen sodium headache pain (source: ndc)
Generic Name
naproxen sodium (source: ndc)
Application Number
ANDA075168 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 220 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (43598-071-01) / 100 TABLET, COATED in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c94f5885-67ab-4e95-df53-a58f119c504b", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["12e45b43-eca2-73f4-1d68-07d4238f8c70"], "manufacturer_name": ["Dr.Reddy's Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (43598-071-01) / 100 TABLET, COATED in 1 BOTTLE", "package_ndc": "43598-071-01", "marketing_start_date": "20211210"}], "brand_name": "Naproxen Sodium Headache Pain", "product_id": "43598-071_c94f5885-67ab-4e95-df53-a58f119c504b", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "43598-071", "generic_name": "Naproxen Sodium", "labeler_name": "Dr.Reddy's Laboratories Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "brand_name_suffix": "Headache Pain", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA075168", "marketing_category": "ANDA", "marketing_start_date": "20211210", "listing_expiration_date": "20261231"}