meclofenamate sodium

Generic: meclofenamate sodium

Labeler: mylan pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name meclofenamate sodium
Generic Name meclofenamate sodium
Labeler mylan pharmaceuticals inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

meclofenamate sodium 50 mg/1

Manufacturer
Mylan Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 0378-2150
Product ID 0378-2150_26f16653-a1af-41b0-8152-6fb9faa96132
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071081
Listing Expiration 2026-12-31
Marketing Start 1986-09-03

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03782150
Hyphenated Format 0378-2150

Supplemental Identifiers

RxCUI
618552 618557
UPC
0303783000015 0303782150018
UNII
94NJ818U2W

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 meclofenamate sodium (source: ndc)
Generic Name meclofenamate sodium (source: ndc)
Application Number ANDA071081 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-2150-01)
source: ndc

Packages (1)

0378-2150-01 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-2150-01)

Ingredients (1)

meclofenamate sodium (50 mg/1)

Linked Drug Pages (1)

Meclofenamate Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "26f16653-a1af-41b0-8152-6fb9faa96132", "openfda": {"upc": ["0303783000015", "0303782150018"], "unii": ["94NJ818U2W"], "rxcui": ["618552", "618557"], "spl_set_id": ["96f19af4-de8f-4fd7-90d8-55fe6ebdd81d"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (0378-2150-01)", "package_ndc": "0378-2150-01", "marketing_start_date": "19860903"}], "brand_name": "Meclofenamate Sodium", "product_id": "0378-2150_26f16653-a1af-41b0-8152-6fb9faa96132", "dosage_form": "CAPSULE", "product_ndc": "0378-2150", "generic_name": "meclofenamate sodium", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclofenamate Sodium", "active_ingredients": [{"name": "MECLOFENAMATE SODIUM", "strength": "50 mg/1"}], "application_number": "ANDA071081", "marketing_category": "ANDA", "marketing_start_date": "19860903", "listing_expiration_date": "20261231"}