Package 63323-842-02

Brand: dicyclomine hydrochloride

Generic: dicyclomine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63323-842-02
Digits Only 6332384202
Product NDC 63323-842
Description

5 VIAL, SINGLE-DOSE in 1 CARTON (63323-842-02) / 2 mL in 1 VIAL, SINGLE-DOSE (63323-842-21)

Marketing

Marketing Status
Marketed Since 2019-09-12
Brand dicyclomine hydrochloride
Generic dicyclomine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "19096abe-de13-44f4-9028-f918519e34f5", "openfda": {"upc": ["0363323842215"], "unii": ["CQ903KQA31"], "rxcui": ["991065"], "spl_set_id": ["350ce812-b9a7-401a-9793-55d2e14bb760"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL, SINGLE-DOSE in 1 CARTON (63323-842-02)  / 2 mL in 1 VIAL, SINGLE-DOSE (63323-842-21)", "package_ndc": "63323-842-02", "marketing_start_date": "20190912"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "63323-842_19096abe-de13-44f4-9028-f918519e34f5", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "63323-842", "generic_name": "Dicyclomine Hydrochloride", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine Hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA210257", "marketing_category": "ANDA", "marketing_start_date": "20190912", "listing_expiration_date": "20261231"}