metoprolol tartrate
Generic: metoprolol tartrate
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
metoprolol tartrate
Generic Name
metoprolol tartrate
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
metoprolol tartrate 100 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43063938
Hyphenated Format
43063-938
Supplemental Identifiers
RxCUI
UPC
UNII
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
source: ndc
Resolved Composition
Strengths
- 100 mg/1
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)
Packages (4)
Ingredients (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"}