naproxen sodium pm

Generic: naproxen sodium

Labeler: strategic sourcing services llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen sodium pm
Generic Name naproxen sodium
Labeler strategic sourcing services llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

diphenhydramine hydrochloride 25 mg/1, naproxen sodium 220 mg/1

Manufacturer
Strategic Sourcing Services LLC

Identifiers & Regulatory

Product NDC 70677-0064
Product ID 70677-0064_eb781b4d-79e1-48e2-b903-57b82e006bef
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA209726
Marketing Start 2018-12-31
Marketing End 2026-12-31

Pharmacologic Class

Classes
anti-inflammatory agents non-steroidal [cs] cyclooxygenase inhibitors [moa] histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc] nonsteroidal anti-inflammatory drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 706770064
Hyphenated Format 70677-0064

Supplemental Identifiers

RxCUI
1550957
UPC
0010939921444
UNII
TC2D6JAD40 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 pm (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA209726 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
  • 220 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (70677-0064-1) / 20 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

70677-0064-1 1 BOTTLE, PLASTIC in 1 BOX (70677-0064-1) / 20 TABLET in 1 BOTTLE, PLASTIC

Ingredients (2)

diphenhydramine hydrochloride (25 mg/1) naproxen sodium (220 mg/1)

Linked Drug Pages (1)

Naproxen Sodium PM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "eb781b4d-79e1-48e2-b903-57b82e006bef", "openfda": {"upc": ["0010939921444"], "unii": ["TC2D6JAD40", "9TN87S3A3C"], "rxcui": ["1550957"], "spl_set_id": ["03a331d8-c957-4949-894f-51d9bd15e0d0"], "manufacturer_name": ["Strategic Sourcing Services LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (70677-0064-1)  / 20 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "70677-0064-1", "marketing_end_date": "20261231", "marketing_start_date": "20181231"}], "brand_name": "Naproxen Sodium PM", "product_id": "70677-0064_eb781b4d-79e1-48e2-b903-57b82e006bef", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "70677-0064", "generic_name": "Naproxen Sodium", "labeler_name": "Strategic Sourcing Services LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium PM", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}, {"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA209726", "marketing_category": "ANDA", "marketing_end_date": "20261231", "marketing_start_date": "20181231"}