Package 51655-940-26
Brand: dicyclomine hydrochloride
Generic: dicyclomine hydrochloridePackage Facts
Identity
Package NDC
51655-940-26
Digits Only
5165594026
Product NDC
51655-940
Description
90 TABLET in 1 BOTTLE, PLASTIC (51655-940-26)
Marketing
Marketing Status
Brand
dicyclomine hydrochloride
Generic
dicyclomine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "497459e7-6d89-87d4-e063-6394a90a052d", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["da82cb46-7b4b-1ef5-e053-2a95a90ad10d"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-940-26)", "package_ndc": "51655-940-26", "marketing_start_date": "20210715"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "51655-940_497459e7-6d89-87d4-e063-6394a90a052d", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "51655-940", "generic_name": "Dicyclomine Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine Hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA040230", "marketing_category": "ANDA", "marketing_start_date": "20210715", "listing_expiration_date": "20271231"}