phenohytro

Generic: phenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromide

Labeler: winder laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name phenohytro
Generic Name phenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromide
Labeler winder laboratories, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

atropine sulfate .0194 mg/1, hyoscyamine sulfate .1037 mg/1, phenobarbital 16.2 mg/1, scopolamine hydrobromide .0065 mg/1

Manufacturer
Winder Laboratories, LLC

Identifiers & Regulatory

Product NDC 75826-118
Product ID 75826-118_2b37a6e2-6e67-1233-e063-6294a90a26ad
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2016-02-29

Pharmacologic Class

Classes
anticholinergic [epc] cholinergic antagonists [moa] cholinergic muscarinic antagonist [epc] cholinergic muscarinic antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 75826118
Hyphenated Format 75826-118

Supplemental Identifiers

RxCUI
1046815 1739887
UPC
0375826118100
UNII
03J5ZE7KA5 F2R8V82B84 YQE403BP4D 451IFR0GXB

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 phenohytro (source: ndc)
Generic Name phenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromide (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .0194 mg/1
  • .1037 mg/1
  • 16.2 mg/1
  • .0065 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE, PLASTIC (75826-118-00)
  • 100 TABLET in 1 BOTTLE, PLASTIC (75826-118-10)
source: ndc

Packages (2)

Ingredients (4)

atropine sulfate (.0194 mg/1) hyoscyamine sulfate (.1037 mg/1) phenobarbital (16.2 mg/1) scopolamine hydrobromide (.0065 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b37a6e2-6e67-1233-e063-6294a90a26ad", "openfda": {"upc": ["0375826118100"], "unii": ["03J5ZE7KA5", "F2R8V82B84", "YQE403BP4D", "451IFR0GXB"], "rxcui": ["1046815", "1739887"], "spl_set_id": ["27c8baac-f8ce-46d8-8a0f-ff769dd408d9"], "manufacturer_name": ["Winder Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (75826-118-00)", "package_ndc": "75826-118-00", "marketing_start_date": "20160229"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (75826-118-10)", "package_ndc": "75826-118-10", "marketing_start_date": "20160229"}], "brand_name": "Phenohytro", "product_id": "75826-118_2b37a6e2-6e67-1233-e063-6294a90a26ad", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "75826-118", "dea_schedule": "CIV", "generic_name": "PHENOBARBITAL, HYOSCYAMINE SULFATE, ATROPINE SULFATE, SCOPOLAMINE HYDROBROMIDE", "labeler_name": "Winder Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenohytro", "active_ingredients": [{"name": "ATROPINE SULFATE", "strength": ".0194 mg/1"}, {"name": "HYOSCYAMINE SULFATE", "strength": ".1037 mg/1"}, {"name": "PHENOBARBITAL", "strength": "16.2 mg/1"}, {"name": "SCOPOLAMINE HYDROBROMIDE", "strength": ".0065 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20160229", "listing_expiration_date": "20261231"}