loxapine

Generic: loxapine

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loxapine
Generic Name loxapine
Labeler actavis pharma, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

loxapine succinate 50 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 0591-0372
Product ID 0591-0372_cae2db34-6be2-45cf-b9b5-9b929650eb4f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072062
Listing Expiration 2026-12-31
Marketing Start 1988-06-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05910372
Hyphenated Format 0591-0372

Supplemental Identifiers

RxCUI
311385 311386 314075 314078
UPC
0305910369019 0305910370015 0305910372019
UNII
X59SG0MRYU

Packaging Origin

Original Packager
true

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 loxapine (source: ndc)
Generic Name loxapine (source: ndc)
Application Number ANDA072062 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE, PLASTIC (0591-0372-01)
source: ndc

Packages (1)

0591-0372-01 100 CAPSULE in 1 BOTTLE, PLASTIC (0591-0372-01)

Ingredients (1)

loxapine succinate (50 mg/1)

Linked Drug Pages (1)

Loxapine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cae2db34-6be2-45cf-b9b5-9b929650eb4f", "openfda": {"upc": ["0305910369019", "0305910370015", "0305910372019"], "unii": ["X59SG0MRYU"], "rxcui": ["311385", "311386", "314075", "314078"], "spl_set_id": ["a6107bb1-3e23-4c5d-bbf4-5e29deff6728"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (0591-0372-01)", "package_ndc": "0591-0372-01", "marketing_start_date": "19880615"}], "brand_name": "Loxapine", "product_id": "0591-0372_cae2db34-6be2-45cf-b9b5-9b929650eb4f", "dosage_form": "CAPSULE", "product_ndc": "0591-0372", "generic_name": "Loxapine", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Loxapine", "active_ingredients": [{"name": "LOXAPINE SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA072062", "marketing_category": "ANDA", "marketing_start_date": "19880615", "listing_expiration_date": "20261231"}