Package 62332-019-30

Brand: meprobamate

Generic: meprobamate
NDC Package

Package Facts

Identity

Package NDC 62332-019-30
Digits Only 6233201930
Product NDC 62332-019
Description

30 TABLET in 1 BOTTLE (62332-019-30)

Marketing

Marketing Status
Marketed Since 2016-03-31
Brand meprobamate
Generic meprobamate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a2f676cd-53ae-4401-9553-a7d70c79bb0a", "openfda": {"unii": ["9I7LNY769Q"], "rxcui": ["197928", "197929"], "spl_set_id": ["3b255bcd-0218-44f8-830b-971f5ec45276"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (62332-019-30)", "package_ndc": "62332-019-30", "marketing_start_date": "20160331"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (62332-019-31)", "package_ndc": "62332-019-31", "marketing_start_date": "20160331"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62332-019-91)", "package_ndc": "62332-019-91", "marketing_start_date": "20160331"}], "brand_name": "Meprobamate", "product_id": "62332-019_a2f676cd-53ae-4401-9553-a7d70c79bb0a", "dosage_form": "TABLET", "product_ndc": "62332-019", "dea_schedule": "CIV", "generic_name": "Meprobamate", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meprobamate", "active_ingredients": [{"name": "MEPROBAMATE", "strength": "200 mg/1"}], "application_number": "ANDA090122", "marketing_category": "ANDA", "marketing_start_date": "20160331", "listing_expiration_date": "20261231"}