Package 67296-2154-1
Brand: dicyclomine hydrochloride
Generic: dicyclomine hydrochloridePackage Facts
Identity
Package NDC
67296-2154-1
Digits Only
6729621541
Product NDC
67296-2154
Description
15 TABLET in 1 BOTTLE (67296-2154-1)
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": "4637deb0-0a45-f07b-e063-6394a90a69fe", "openfda": {"unii": ["CQ903KQA31"], "rxcui": ["991086"], "spl_set_id": ["3252540c-980d-40ca-e063-6394a90ad1c9"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (67296-2154-1)", "package_ndc": "67296-2154-1", "marketing_start_date": "20230425"}], "brand_name": "Dicyclomine Hydrochloride", "product_id": "67296-2154_4637deb0-0a45-f07b-e063-6394a90a69fe", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "67296-2154", "generic_name": "Dicyclomine Hydrochloride", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dicyclomine Hydrochloride", "active_ingredients": [{"name": "DICYCLOMINE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA040317", "marketing_category": "ANDA", "marketing_start_date": "20230425", "listing_expiration_date": "20261231"}