Package 72319-029-06
Brand: methscopolamine bromide
Generic: methscopolamine bromidePackage Facts
Identity
Package NDC
72319-029-06
Digits Only
7231902906
Product NDC
72319-029
Description
1000 TABLET in 1 BOTTLE (72319-029-06)
Marketing
Marketing Status
Brand
methscopolamine bromide
Generic
methscopolamine bromide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2ee941f2-7d8c-dd6e-e063-6394a90a0db9", "openfda": {"unii": ["RTN51LK7WL"], "rxcui": ["314088", "403914"], "spl_set_id": ["14c0c030-e96d-4a5e-95ff-02dd78a46be3"], "manufacturer_name": ["i3 Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72319-029-04)", "package_ndc": "72319-029-04", "marketing_start_date": "20241218"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (72319-029-06)", "package_ndc": "72319-029-06", "marketing_start_date": "20241218"}], "brand_name": "METHSCOPOLAMINE BROMIDE", "product_id": "72319-029_2ee941f2-7d8c-dd6e-e063-6394a90a0db9", "dosage_form": "TABLET", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]"], "product_ndc": "72319-029", "generic_name": "methscopolamine bromide", "labeler_name": "i3 Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHSCOPOLAMINE BROMIDE", "active_ingredients": [{"name": "METHSCOPOLAMINE BROMIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA216786", "marketing_category": "ANDA", "marketing_start_date": "20241218", "listing_expiration_date": "20261231"}