arthritis pain reliever

Generic: diclofenac sodium

Labeler: h e b
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name arthritis pain reliever
Generic Name diclofenac sodium
Labeler h e b
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

diclofenac sodium 10 mg/g

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-087
Product ID 37808-087_a0bb2dd0-1a91-452e-83dd-61c717c39530
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211253
Listing Expiration 2026-12-31
Marketing Start 2020-08-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808087
Hyphenated Format 37808-087

Supplemental Identifiers

RxCUI
855633
UNII
QTG126297Q

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 arthritis pain reliever (source: ndc)
Generic Name diclofenac sodium (source: ndc)
Application Number ANDA211253 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (37808-087-01) / 100 g in 1 TUBE
  • 1 TUBE in 1 CARTON (37808-087-02) / 50 g in 1 TUBE
  • 1 TUBE in 1 CARTON (37808-087-03) / 150 g in 1 TUBE
source: ndc

Packages (3)

37808-087-01 1 TUBE in 1 CARTON (37808-087-01) / 100 g in 1 TUBE 37808-087-02 1 TUBE in 1 CARTON (37808-087-02) / 50 g in 1 TUBE 37808-087-03 1 TUBE in 1 CARTON (37808-087-03) / 150 g in 1 TUBE

Ingredients (1)

diclofenac sodium (10 mg/g)

Linked Drug Pages (1)

arthritis pain reliever ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "a0bb2dd0-1a91-452e-83dd-61c717c39530", "openfda": {"unii": ["QTG126297Q"], "rxcui": ["855633"], "spl_set_id": ["e8fe4a89-586d-461c-b242-b68e38a508b4"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (37808-087-01)  / 100 g in 1 TUBE", "package_ndc": "37808-087-01", "marketing_start_date": "20200806"}, {"sample": false, "description": "1 TUBE in 1 CARTON (37808-087-02)  / 50 g in 1 TUBE", "package_ndc": "37808-087-02", "marketing_start_date": "20201112"}, {"sample": false, "description": "1 TUBE in 1 CARTON (37808-087-03)  / 150 g in 1 TUBE", "package_ndc": "37808-087-03", "marketing_start_date": "20201118"}], "brand_name": "arthritis pain reliever", "product_id": "37808-087_a0bb2dd0-1a91-452e-83dd-61c717c39530", "dosage_form": "GEL", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Prostaglandin Production [PE]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "37808-087", "generic_name": "diclofenac sodium", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "arthritis pain reliever", "active_ingredients": [{"name": "DICLOFENAC SODIUM", "strength": "10 mg/g"}], "application_number": "ANDA211253", "marketing_category": "ANDA", "marketing_start_date": "20200806", "listing_expiration_date": "20261231"}