Package 46708-019-71

Brand: meprobamate

Generic: meprobamate
NDC Package

Package Facts

Identity

Package NDC 46708-019-71
Digits Only 4670801971
Product NDC 46708-019
Description

100 TABLET in 1 BOTTLE (46708-019-71)

Marketing

Marketing Status
Marketed Since 2013-07-23
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": "8c5c7ad8-a128-4243-bd03-0e7057295b3f", "openfda": {"upc": ["0346708020309", "0346708019303"], "unii": ["9I7LNY769Q"], "rxcui": ["197928", "197929"], "spl_set_id": ["a0891a32-105b-48bc-a246-5e179d2e7fa1"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (46708-019-30)", "package_ndc": "46708-019-30", "marketing_start_date": "20130723"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (46708-019-71)", "package_ndc": "46708-019-71", "marketing_start_date": "20130723"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (46708-019-91)", "package_ndc": "46708-019-91", "marketing_start_date": "20130723"}], "brand_name": "MEPROBAMATE", "product_id": "46708-019_8c5c7ad8-a128-4243-bd03-0e7057295b3f", "dosage_form": "TABLET", "product_ndc": "46708-019", "dea_schedule": "CIV", "generic_name": "MEPROBAMATE", "labeler_name": "Alembic Pharmaceuticals Limited", "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": "20130723", "listing_expiration_date": "20261231"}