naproxen sodium headache pain

Generic: naproxen sodium

Labeler: dr.reddy's laboratories inc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen sodium headache pain
Generic Name naproxen sodium
Labeler dr.reddy's laboratories inc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Dr.Reddy's Laboratories Inc

Identifiers & Regulatory

Product NDC 43598-072
Product ID 43598-072_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
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 43598072
Hyphenated Format 43598-072

Supplemental Identifiers

RxCUI
849574
UNII
9TN87S3A3C

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 naproxen sodium headache pain (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA075168 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (43598-072-01) / 100 TABLET, COATED in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

naproxen sodium (220 mg/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 (43598-072-01)  / 100 TABLET, COATED in 1 BOTTLE", "package_ndc": "43598-072-01", "marketing_start_date": "20211210"}], "brand_name": "Naproxen Sodium Headache Pain", "product_id": "43598-072_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": "43598-072", "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"}