metoprolol tartrate

Generic: metoprolol tartrate

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metoprolol tartrate
Generic Name metoprolol tartrate
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metoprolol tartrate 100 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-938
Product ID 43063-938_415ead07-5bf7-51fc-e063-6294a90a4c4d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077739
Listing Expiration 2026-12-31
Marketing Start 2007-09-11

Pharmacologic Class

Classes
adrenergic beta-antagonists [moa] beta-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43063938
Hyphenated Format 43063-938

Supplemental Identifiers

RxCUI
866511
UPC
0343063938935
UNII
W5S57Y3A5L

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 metoprolol tartrate (source: ndc)
Generic Name metoprolol tartrate (source: ndc)
Application Number ANDA077739 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-938-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-938-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-938-90)
  • 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-938-93)
source: ndc

Packages (4)

Ingredients (1)

metoprolol tartrate (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "415ead07-5bf7-51fc-e063-6294a90a4c4d", "openfda": {"upc": ["0343063938935"], "unii": ["W5S57Y3A5L"], "rxcui": ["866511"], "spl_set_id": ["f4a4da81-c4d0-4a00-9f08-9029b5d9b5ea"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-938-30)", "package_ndc": "43063-938-30", "marketing_start_date": "20190513"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-938-60)", "package_ndc": "43063-938-60", "marketing_start_date": "20190316"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-938-90)", "package_ndc": "43063-938-90", "marketing_start_date": "20190129"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-938-93)", "package_ndc": "43063-938-93", "marketing_start_date": "20190129"}], "brand_name": "Metoprolol Tartrate", "product_id": "43063-938_415ead07-5bf7-51fc-e063-6294a90a4c4d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "43063-938", "generic_name": "Metoprolol Tartrate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metoprolol Tartrate", "active_ingredients": [{"name": "METOPROLOL TARTRATE", "strength": "100 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_start_date": "20070911", "listing_expiration_date": "20261231"}