Package 43386-581-31
Brand: metoclopramide hydrochloride
Generic: metoclopramide hydrochloridePackage Facts
Identity
Package NDC
43386-581-31
Digits Only
4338658131
Product NDC
43386-581
Description
1 BLISTER PACK in 1 CARTON (43386-581-31) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Marketing
Marketing Status
Brand
metoclopramide hydrochloride
Generic
metoclopramide hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b5844be2-94b3-3e3f-e053-2995a90a6eb8", "openfda": {"unii": ["W1792A2RVD"], "rxcui": ["608623", "608624"], "spl_set_id": ["7cd1dc35-2fb2-4f1d-8769-24c3c3aa34fa"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (43386-581-31) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "43386-581-31", "marketing_start_date": "20150406"}], "brand_name": "METOCLOPRAMIDE hydrochloride", "product_id": "43386-581_b5844be2-94b3-3e3f-e053-2995a90a6eb8", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Dopamine D2 Antagonists [MoA]", "Dopamine-2 Receptor Antagonist [EPC]"], "product_ndc": "43386-581", "generic_name": "Metoclopramide Hydrochloride", "labeler_name": "Lupin Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METOCLOPRAMIDE hydrochloride", "active_ingredients": [{"name": "METOCLOPRAMIDE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA202191", "marketing_category": "ANDA", "marketing_start_date": "20150406", "listing_expiration_date": "20261231"}