phenohytro
Generic: phenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromide
Labeler: winder laboratories, llcDrug Facts
Product Profile
Brand Name
phenohytro
Generic Name
phenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromide
Labeler
winder laboratories, llc
Dosage Form
TABLET
Routes
Active Ingredients
atropine sulfate .0194 mg/1, hyoscyamine sulfate .1037 mg/1, phenobarbital 16.2 mg/1, scopolamine hydrobromide .0065 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
75826118
Hyphenated Format
75826-118
Supplemental Identifiers
RxCUI
UPC
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
phenohytro (source: ndc)
Generic Name
phenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromide (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .0194 mg/1
- .1037 mg/1
- 16.2 mg/1
- .0065 mg/1
Packaging
- 1000 TABLET in 1 BOTTLE, PLASTIC (75826-118-00)
- 100 TABLET in 1 BOTTLE, PLASTIC (75826-118-10)
Packages (2)
Ingredients (4)
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"}