0591-0605
Generic: labetalol hydrochloride
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
Generic Name
labetalol hydrochloride
Labeler
actavis pharma, inc.
Dosage Form
TABLET, FILM COATED
Active Ingredients
labetalol hydrochloride 100 mg/1
Identifiers & Regulatory
Product NDC
0591-0605
Product ID
0591-0605_5f610138-2bdd-4cc8-aa9d-26a7d67c6ffa
Product Type
DRUG FOR FURTHER PROCESSING
Marketing Category
DRUG FOR FURTHER PROCESSING
Marketing Start
1998-08-03
Marketing End
2026-09-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05910605
Hyphenated Format
0591-0605
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
labetalol hydrochloride (source: label)
Generic Name
labetalol hydrochloride (source: ndc)
Application Number
ANDA075133 (source: label)
Routes
source: label
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 64700 TABLET, FILM COATED in 1 BAG (0591-0605-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "5f610138-2bdd-4cc8-aa9d-26a7d67c6ffa", "openfda": {}, "finished": false, "packaging": [{"description": "64700 TABLET, FILM COATED in 1 BAG (0591-0605-00)", "package_ndc": "0591-0605-00", "marketing_end_date": "30-SEP-26", "marketing_start_date": "03-AUG-98"}], "product_id": "0591-0605_5f610138-2bdd-4cc8-aa9d-26a7d67c6ffa", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0591-0605", "generic_name": "Labetalol hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "DRUG FOR FURTHER PROCESSING", "brand_name_base": null, "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "100 mg/1"}], "marketing_category": "DRUG FOR FURTHER PROCESSING", "marketing_end_date": "20260930", "marketing_start_date": "19980803"}