Package 0093-2204-01
Brand: metoclopramide
Generic: metoclopramidePackage Facts
Identity
Package NDC
0093-2204-01
Digits Only
0093220401
Product NDC
0093-2204
Description
100 TABLET in 1 BOTTLE (0093-2204-01)
Marketing
Marketing Status
Brand
metoclopramide
Generic
metoclopramide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8f208d35-b19b-40a1-b363-f44ff08ec3d6", "openfda": {"upc": ["0300932204010", "0300932203013"], "unii": ["W1792A2RVD"], "rxcui": ["311666", "311668"], "spl_set_id": ["e15905e0-e0f6-4c8b-ac19-59724d6c4bf0"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0093-2204-01)", "package_ndc": "0093-2204-01", "marketing_start_date": "19930701"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0093-2204-05)", "package_ndc": "0093-2204-05", "marketing_start_date": "19930701"}], "brand_name": "Metoclopramide", "product_id": "0093-2204_8f208d35-b19b-40a1-b363-f44ff08ec3d6", "dosage_form": "TABLET", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "0093-2204", "generic_name": "Metoclopramide", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoclopramide", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA072801", "marketing_category": "ANDA", "marketing_start_date": "19930701", "listing_expiration_date": "20261231"}