8 hr arthritis pain relief

Generic: acetaminophen

Labeler: dolgencorp, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name 8 hr arthritis pain relief
Generic Name acetaminophen
Labeler dolgencorp, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
DOLGENCORP, INC.

Identifiers & Regulatory

Product NDC 55910-892
Product ID 55910-892_f9c20045-2698-d9b2-e053-6294a90a2b11
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA215486
Listing Expiration 2026-12-31
Marketing Start 2023-04-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55910892
Hyphenated Format 55910-892

Supplemental Identifiers

RxCUI
1148399
UPC
0355910892420 0355910892260 0355910892055
UNII
362O9ITL9D

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 8 hr arthritis pain relief (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number ANDA215486 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (55910-892-05) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (55910-892-26) / 225 TABLET, EXTENDED RELEASE in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (55910-892-42) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE
source: ndc

Packages (3)

55910-892-05 1 BOTTLE in 1 CARTON (55910-892-05) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE 55910-892-26 1 BOTTLE in 1 CARTON (55910-892-26) / 225 TABLET, EXTENDED RELEASE in 1 BOTTLE 55910-892-42 1 BOTTLE in 1 CARTON (55910-892-42) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

8 hr Arthritis Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f9c20045-2698-d9b2-e053-6294a90a2b11", "openfda": {"upc": ["0355910892420", "0355910892260", "0355910892055"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["ea2eae7c-e9bd-534c-e053-2a95a90a26c8"], "manufacturer_name": ["DOLGENCORP, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (55910-892-05)  / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "55910-892-05", "marketing_start_date": "20230429"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (55910-892-26)  / 225 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "55910-892-26", "marketing_start_date": "20230429"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (55910-892-42)  / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "55910-892-42", "marketing_start_date": "20230429"}], "brand_name": "8 hr Arthritis Pain Relief", "product_id": "55910-892_f9c20045-2698-d9b2-e053-6294a90a2b11", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "55910-892", "generic_name": "Acetaminophen", "labeler_name": "DOLGENCORP, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "8 hr Arthritis Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA215486", "marketing_category": "ANDA", "marketing_start_date": "20230429", "listing_expiration_date": "20261231"}