members mark acetaminophen
Generic: acetaminophen
Labeler: sam's west incDrug Facts
Product Profile
Brand Name
members mark acetaminophen
Generic Name
acetaminophen
Labeler
sam's west inc
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68196-606
Product ID
68196-606_7ffc4074-36e3-464a-ab67-6661f72a7b60
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2025-11-20
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68196606
Hyphenated Format
68196-606
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
members mark acetaminophen (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 600 TABLET in 1 BOTTLE (68196-606-61)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7ffc4074-36e3-464a-ab67-6661f72a7b60", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["03e831d4-8060-4633-9d02-e77100063fb4"], "manufacturer_name": ["Sam's West Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "600 TABLET in 1 BOTTLE (68196-606-61)", "package_ndc": "68196-606-61", "marketing_start_date": "20251120"}], "brand_name": "MEMBERS MARK ACETAMINOPHEN", "product_id": "68196-606_7ffc4074-36e3-464a-ab67-6661f72a7b60", "dosage_form": "TABLET", "product_ndc": "68196-606", "generic_name": "Acetaminophen", "labeler_name": "Sam's West Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MEMBERS MARK ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251120", "listing_expiration_date": "20261231"}