bronkaid max

Generic: ephedrine sulfate

Labeler: foundation consumer healthcare llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name bronkaid max
Generic Name ephedrine sulfate
Labeler foundation consumer healthcare llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

ephedrine sulfate 25 mg/1

Manufacturer
Foundation Consumer Healthcare LLC

Identifiers & Regulatory

Product NDC 69536-250
Product ID 69536-250_e406ff56-f8d4-49e8-b5ba-8c94bcf8052f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2020-09-01

Pharmacologic Class

Classes
adrenergic alpha-agonists [moa] adrenergic beta-agonists [moa] increased norepinephrine activity [pe] norepinephrine releasing agent [epc] alpha-adrenergic agonist [epc] beta-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69536250
Hyphenated Format 69536-250

Supplemental Identifiers

RxCUI
1116194 2396449
UNII
U6X61U5ZEG

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 bronkaid max (source: ndc)
Generic Name ephedrine sulfate (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 4 BLISTER PACK in 1 CARTON (69536-250-24) / 6 TABLET, COATED in 1 BLISTER PACK
  • 5 BLISTER PACK in 1 CARTON (69536-250-60) / 12 TABLET, COATED in 1 BLISTER PACK
source: ndc

Packages (2)

69536-250-24 4 BLISTER PACK in 1 CARTON (69536-250-24) / 6 TABLET, COATED in 1 BLISTER PACK 69536-250-60 5 BLISTER PACK in 1 CARTON (69536-250-60) / 12 TABLET, COATED in 1 BLISTER PACK

Ingredients (1)

ephedrine sulfate (25 mg/1)

Linked Drug Pages (1)

Bronkaid Max ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e406ff56-f8d4-49e8-b5ba-8c94bcf8052f", "openfda": {"unii": ["U6X61U5ZEG"], "rxcui": ["1116194", "2396449"], "spl_set_id": ["9a0b792a-caee-41f6-9400-922a5ebd592f"], "manufacturer_name": ["Foundation Consumer Healthcare LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (69536-250-24)  / 6 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "69536-250-24", "marketing_start_date": "20200901"}, {"sample": false, "description": "5 BLISTER PACK in 1 CARTON (69536-250-60)  / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "69536-250-60", "marketing_start_date": "20200901"}], "brand_name": "Bronkaid Max", "product_id": "69536-250_e406ff56-f8d4-49e8-b5ba-8c94bcf8052f", "dosage_form": "TABLET, COATED", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Adrenergic beta-Agonists [MoA]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Releasing Agent [EPC]", "alpha-Adrenergic Agonist [EPC]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "69536-250", "generic_name": "EPHEDRINE SULFATE", "labeler_name": "Foundation Consumer Healthcare LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bronkaid", "brand_name_suffix": "Max", "active_ingredients": [{"name": "EPHEDRINE SULFATE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200901", "listing_expiration_date": "20261231"}