meprobamate

Generic: meprobamate

Labeler: alembic pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name meprobamate
Generic Name meprobamate
Labeler alembic pharmaceuticals limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meprobamate 200 mg/1

Manufacturer
Alembic Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 46708-019
Product ID 46708-019_8c5c7ad8-a128-4243-bd03-0e7057295b3f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090122
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2013-07-23

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 46708019
Hyphenated Format 46708-019

Supplemental Identifiers

RxCUI
197928 197929
UPC
0346708020309 0346708019303
UNII
9I7LNY769Q

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name meprobamate (source: ndc)
Generic Name meprobamate (source: ndc)
Application Number ANDA090122 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (46708-019-30)
  • 100 TABLET in 1 BOTTLE (46708-019-71)
  • 1000 TABLET in 1 BOTTLE (46708-019-91)
source: ndc

Packages (3)

46708-019-30 30 TABLET in 1 BOTTLE (46708-019-30) 46708-019-71 100 TABLET in 1 BOTTLE (46708-019-71) 46708-019-91 1000 TABLET in 1 BOTTLE (46708-019-91)

Ingredients (1)

meprobamate (200 mg/1)

Linked Drug Pages (1)

MEPROBAMATE ndc-match (0.9)

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"}