pindolol
Generic: pindolol
Labeler: sun pharmaceutical industries, inc.Drug Facts
Product Profile
Brand Name
pindolol
Generic Name
pindolol
Labeler
sun pharmaceutical industries, inc.
Dosage Form
TABLET
Routes
Active Ingredients
pindolol 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
57664-656
Product ID
57664-656_a0a57e6d-d85e-46df-b564-bc522691031a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074063
Listing Expiration
2026-12-31
Marketing Start
1994-01-27
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
57664656
Hyphenated Format
57664-656
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
pindolol (source: ndc)
Generic Name
pindolol (source: ndc)
Application Number
ANDA074063 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 TABLET in 1 BOTTLE, PLASTIC (57664-656-88)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a0a57e6d-d85e-46df-b564-bc522691031a", "openfda": {"nui": ["N0000000161", "N0000175556"], "upc": ["0357664656884", "0357664655887"], "unii": ["BJ4HF6IU1D"], "rxcui": ["198104", "198105"], "spl_set_id": ["b331a73f-bf7b-4442-8901-36d016530279"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (57664-656-88)", "package_ndc": "57664-656-88", "marketing_start_date": "19940127"}], "brand_name": "Pindolol", "product_id": "57664-656_a0a57e6d-d85e-46df-b564-bc522691031a", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "57664-656", "generic_name": "Pindolol", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pindolol", "active_ingredients": [{"name": "PINDOLOL", "strength": "10 mg/1"}], "application_number": "ANDA074063", "marketing_category": "ANDA", "marketing_start_date": "19940127", "listing_expiration_date": "20261231"}