dimenhydrinate

Generic: dimenhydrinate

Labeler: major pharmaceuticals
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name dimenhydrinate
Generic Name dimenhydrinate
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dimenhydrinate 50 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6772
Product ID 0904-6772_3c44729b-0a55-8eaf-e063-6394a90a5ba4
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M009
Marketing Start 2019-02-14
Marketing End 2028-08-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09046772
Hyphenated Format 0904-6772

Supplemental Identifiers

RxCUI
198603
UPC
0309046772125
UNII
JB937PER5C

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 dimenhydrinate (source: ndc)
Generic Name dimenhydrinate (source: ndc)
Application Number M009 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (0904-6772-12) / 12 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0904-6772-12 1 BLISTER PACK in 1 CARTON (0904-6772-12) / 12 TABLET in 1 BLISTER PACK

Ingredients (1)

dimenhydrinate (50 mg/1)

Linked Drug Pages (1)

Dimenhydrinate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3c44729b-0a55-8eaf-e063-6394a90a5ba4", "openfda": {"upc": ["0309046772125"], "unii": ["JB937PER5C"], "rxcui": ["198603"], "spl_set_id": ["78d22836-a442-7c0c-e053-2991aa0a62f3"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0904-6772-12)  / 12 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6772-12", "marketing_end_date": "20280831", "marketing_start_date": "20190214"}], "brand_name": "Dimenhydrinate", "product_id": "0904-6772_3c44729b-0a55-8eaf-e063-6394a90a5ba4", "dosage_form": "TABLET", "product_ndc": "0904-6772", "generic_name": "Dimenhydrinate", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dimenhydrinate", "active_ingredients": [{"name": "DIMENHYDRINATE", "strength": "50 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20280831", "marketing_start_date": "20190214"}