Package 63323-366-01

Brand: dimenhydrinate

Generic: dimenhydrinate
NDC Package

Package Facts

Identity

Package NDC 63323-366-01
Digits Only 6332336601
Product NDC 63323-366
Product ID 63323-366_b3e3433d-c18b-4ed3-b2ba-1e550474ca33
Description

25 VIAL in 1 TRAY (63323-366-01) / 1 mL in 1 VIAL (63323-366-00)

Marketing

Marketing Status
Marketed Since 2004-11-29
Brand dimenhydrinate
Generic dimenhydrinate
Sample Package No

Linked Drug Pages (1)

Dimenhydrinate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "b3e3433d-c18b-4ed3-b2ba-1e550474ca33", "openfda": {"upc": ["0363323366001"], "unii": ["JB937PER5C"], "rxcui": ["309914"], "spl_set_id": ["bc71539e-1a33-4709-8a24-c2894e8dbc1c"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 TRAY (63323-366-01)  / 1 mL in 1 VIAL (63323-366-00)", "package_ndc": "63323-366-01", "marketing_start_date": "20041129"}], "brand_name": "Dimenhydrinate", "product_id": "63323-366_b3e3433d-c18b-4ed3-b2ba-1e550474ca33", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "63323-366", "generic_name": "Dimenhydrinate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dimenhydrinate", "active_ingredients": [{"name": "DIMENHYDRINATE", "strength": "50 mg/mL"}], "application_number": "ANDA040519", "marketing_category": "ANDA", "marketing_start_date": "20041129", "listing_expiration_date": "20261231"}