axiv daytime - liquid

Generic: acetaminophen, dextromethorphan hydrobromide

Labeler: vivunt pharma llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name axiv daytime - liquid
Generic Name acetaminophen, dextromethorphan hydrobromide
Labeler vivunt pharma llc
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/30mL, dextromethorphan hydrobromide 20 mg/30mL

Manufacturer
VIVUNT PHARMA LLC

Identifiers & Regulatory

Product NDC 82706-022
Product ID 82706-022_3f018b49-e425-34a4-e063-6294a90adfa0
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2024-05-14

Pharmacologic Class

Classes
sigma-1 agonist [epc] sigma-1 receptor agonists [moa] uncompetitive n-methyl-d-aspartate receptor antagonist [epc] uncompetitive nmda receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82706022
Hyphenated Format 82706-022

Supplemental Identifiers

RxCUI
2604561
UPC
0850047780638
UNII
362O9ITL9D 9D2RTI9KYH

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 axiv daytime - liquid (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/30mL
  • 20 mg/30mL
source: ndc
Packaging
  • 355 mL in 1 BOTTLE, PLASTIC (82706-022-01)
source: ndc

Packages (1)

82706-022-01 355 mL in 1 BOTTLE, PLASTIC (82706-022-01)

Ingredients (2)

acetaminophen (650 mg/30mL) dextromethorphan hydrobromide (20 mg/30mL)

Linked Drug Pages (1)

AXIV DayTime - Liquid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f018b49-e425-34a4-e063-6294a90adfa0", "openfda": {"upc": ["0850047780638"], "unii": ["362O9ITL9D", "9D2RTI9KYH"], "rxcui": ["2604561"], "spl_set_id": ["1872e1ff-2e08-c404-e063-6294a90afa14"], "manufacturer_name": ["VIVUNT PHARMA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE, PLASTIC (82706-022-01)", "package_ndc": "82706-022-01", "marketing_start_date": "20240514"}], "brand_name": "AXIV DayTime - Liquid", "product_id": "82706-022_3f018b49-e425-34a4-e063-6294a90adfa0", "dosage_form": "LIQUID", "pharm_class": ["Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "82706-022", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide", "labeler_name": "VIVUNT PHARMA LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "AXIV DayTime - Liquid", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/30mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/30mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240514", "listing_expiration_date": "20261231"}