medi-first non-aspirin
Generic: acetaminophen
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
medi-first non-aspirin
Generic Name
acetaminophen
Labeler
proficient rx lp
Dosage Form
TABLET, COATED
Routes
Active Ingredients
acetaminophen 325 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-306
Product ID
71205-306_4eb6a025-a57e-46fa-938b-25c93d4627aa
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2008-12-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205306
Hyphenated Format
71205-306
Supplemental Identifiers
RxCUI
UNII
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
medi-first non-aspirin (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
Packaging
- 4 TABLET, COATED in 1 PACKET (71205-306-04)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4eb6a025-a57e-46fa-938b-25c93d4627aa", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["313782"], "spl_set_id": ["4c84948d-3a95-4c53-8529-7e7b9d8bb6df"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, COATED in 1 PACKET (71205-306-04)", "package_ndc": "71205-306-04", "marketing_start_date": "20190801"}], "brand_name": "MEDI-FIRST Non-Aspirin", "product_id": "71205-306_4eb6a025-a57e-46fa-938b-25c93d4627aa", "dosage_form": "TABLET, COATED", "product_ndc": "71205-306", "generic_name": "Acetaminophen", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MEDI-FIRST Non-Aspirin", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20081230", "listing_expiration_date": "20261231"}