antigrip nighttime
Generic: acetaminophen, dextromethorphan hbr, doxylamine succinate, phenylephrine hcl
Labeler: pharmadel llcDrug Facts
Product Profile
Brand Name
antigrip nighttime
Generic Name
acetaminophen, dextromethorphan hbr, doxylamine succinate, phenylephrine hcl
Labeler
pharmadel llc
Dosage Form
POWDER, FOR SOLUTION
Routes
Active Ingredients
acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1, doxylamine succinate 6.25 mg/1, phenylephrine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55758-382
Product ID
55758-382_14ac7b0a-30d9-e209-e063-6394a90a5c14
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2024-03-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55758382
Hyphenated Format
55758-382
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
antigrip nighttime (source: ndc)
Generic Name
acetaminophen, dextromethorphan hbr, doxylamine succinate, phenylephrine hcl (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 10 mg/1
- 6.25 mg/1
- 5 mg/1
Packaging
- 18 POUCH in 1 CARTON (55758-382-18) / 1 POWDER, FOR SOLUTION in 1 POUCH (55758-382-01)
Packages (1)
Ingredients (4)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "14ac7b0a-30d9-e209-e063-6394a90a5c14", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "V9BI9B5YI2", "04JA59TNSJ"], "rxcui": ["2677914"], "spl_set_id": ["12de30fd-95b6-f16d-e063-6294a90aeba2"], "manufacturer_name": ["Pharmadel LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "18 POUCH in 1 CARTON (55758-382-18) / 1 POWDER, FOR SOLUTION in 1 POUCH (55758-382-01)", "package_ndc": "55758-382-18", "marketing_start_date": "20240328"}], "brand_name": "ANTIGRIP Nighttime", "product_id": "55758-382_14ac7b0a-30d9-e209-e063-6394a90a5c14", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "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]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "55758-382", "generic_name": "Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCL", "labeler_name": "Pharmadel LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ANTIGRIP", "brand_name_suffix": "Nighttime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "DOXYLAMINE SUCCINATE", "strength": "6.25 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240328", "listing_expiration_date": "20261231"}