axiv nighttime

Generic: acetaminophen, dextromethorphan hydrobromide, doxylamine succinate

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

Drug Facts

Product Profile

Brand Name axiv nighttime
Generic Name acetaminophen, dextromethorphan hydrobromide, doxylamine succinate
Labeler vivunt pharma llc
Dosage Form CAPSULE, LIQUID FILLED
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, dextromethorphan hydrobromide 15 mg/1, doxylamine succinate 6.25 mg/1

Manufacturer
VIVUNT PHARMA LLC

Identifiers & Regulatory

Product NDC 82706-016
Product ID 82706-016_3f047bdc-549e-c77b-e063-6394a90ae7ad
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2024-03-07

Pharmacologic Class

Classes
antihistamine [epc] histamine receptor antagonists [moa] 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 82706016
Hyphenated Format 82706-016

Supplemental Identifiers

RxCUI
1094549
UPC
0850047780591 0850047780379 0850047780416
UNII
362O9ITL9D 9D2RTI9KYH V9BI9B5YI2

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 nighttime (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, doxylamine succinate (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 15 mg/1
  • 6.25 mg/1
source: ndc
Packaging
  • 3 BLISTER PACK in 1 CARTON (82706-016-01) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
  • 50 POUCH in 1 CARTON (82706-016-03) / 2 CAPSULE, LIQUID FILLED in 1 POUCH
  • 25 BLISTER PACK in 1 CARTON (82706-016-04) / 25 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
source: ndc

Packages (3)

Ingredients (3)

acetaminophen (325 mg/1) dextromethorphan hydrobromide (15 mg/1) doxylamine succinate (6.25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f047bdc-549e-c77b-e063-6394a90ae7ad", "openfda": {"upc": ["0850047780591", "0850047780379", "0850047780416"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "V9BI9B5YI2"], "rxcui": ["1094549"], "spl_set_id": ["131f6314-c9a1-7af3-e063-6294a90abe6f"], "manufacturer_name": ["VIVUNT PHARMA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (82706-016-01)  / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "82706-016-01", "marketing_start_date": "20240307"}, {"sample": false, "description": "50 POUCH in 1 CARTON (82706-016-03)  / 2 CAPSULE, LIQUID FILLED in 1 POUCH", "package_ndc": "82706-016-03", "marketing_start_date": "20240705"}, {"sample": false, "description": "25 BLISTER PACK in 1 CARTON (82706-016-04)  / 25 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "82706-016-04", "marketing_start_date": "20250212"}], "brand_name": "AXIV NightTime", "product_id": "82706-016_3f047bdc-549e-c77b-e063-6394a90ae7ad", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "82706-016", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate", "labeler_name": "VIVUNT PHARMA LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "AXIV NightTime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "15 mg/1"}, {"name": "DOXYLAMINE SUCCINATE", "strength": "6.25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240307", "listing_expiration_date": "20261231"}