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 50 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-821
Product ID 43063-821_47cee106-d10c-fb07-e063-6294a90ac517
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077739
Marketing Start 2007-09-11
Marketing End 2027-08-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43063821
Hyphenated Format 43063-821

Supplemental Identifiers

RxCUI
866514
UPC
0343063821305
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
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-90)
  • 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-93)
source: ndc

Packages (4)

43063-821-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-30) 43063-821-60 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-60) 43063-821-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-90) 43063-821-93 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-93)

Ingredients (1)

metoprolol tartrate (50 mg/1)

Linked Drug Pages (1)

Metoprolol Tartrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47cee106-d10c-fb07-e063-6294a90ac517", "openfda": {"upc": ["0343063821305"], "unii": ["W5S57Y3A5L"], "rxcui": ["866514"], "spl_set_id": ["19678edf-934a-45f3-b5da-94d10e9b3248"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-30)", "package_ndc": "43063-821-30", "marketing_end_date": "20270831", "marketing_start_date": "20180627"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-60)", "package_ndc": "43063-821-60", "marketing_end_date": "20270831", "marketing_start_date": "20180517"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-90)", "package_ndc": "43063-821-90", "marketing_end_date": "20270831", "marketing_start_date": "20170105"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-93)", "package_ndc": "43063-821-93", "marketing_end_date": "20270831", "marketing_start_date": "20170105"}], "brand_name": "Metoprolol Tartrate", "product_id": "43063-821_47cee106-d10c-fb07-e063-6294a90ac517", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "43063-821", "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": "50 mg/1"}], "application_number": "ANDA077739", "marketing_category": "ANDA", "marketing_end_date": "20270831", "marketing_start_date": "20070911"}