loxapine

Generic: loxapine

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loxapine
Generic Name loxapine
Labeler lannett company, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

loxapine succinate 50 mg/1

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 0527-1397
Product ID 0527-1397_d237714b-55f8-4a6e-9297-c10d41ab3cd2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090695
Listing Expiration 2026-12-31
Marketing Start 2011-09-26

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05271397
Hyphenated Format 0527-1397

Supplemental Identifiers

RxCUI
311385 311386 314075 314078
UPC
0305271397010 0305271396013
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 ANDA090695 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE, PLASTIC (0527-1397-01)
  • 1000 CAPSULE in 1 BOTTLE, PLASTIC (0527-1397-10)
source: ndc

Packages (2)

0527-1397-01 100 CAPSULE in 1 BOTTLE, PLASTIC (0527-1397-01) 0527-1397-10 1000 CAPSULE in 1 BOTTLE, PLASTIC (0527-1397-10)

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": "d237714b-55f8-4a6e-9297-c10d41ab3cd2", "openfda": {"upc": ["0305271397010", "0305271396013"], "unii": ["X59SG0MRYU"], "rxcui": ["311385", "311386", "314075", "314078"], "spl_set_id": ["509bad3c-b563-4042-b270-d28bde19f224"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (0527-1397-01)", "package_ndc": "0527-1397-01", "marketing_start_date": "20110926"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE, PLASTIC (0527-1397-10)", "package_ndc": "0527-1397-10", "marketing_start_date": "20110926"}], "brand_name": "Loxapine", "product_id": "0527-1397_d237714b-55f8-4a6e-9297-c10d41ab3cd2", "dosage_form": "CAPSULE", "product_ndc": "0527-1397", "generic_name": "Loxapine", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Loxapine", "active_ingredients": [{"name": "LOXAPINE SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA090695", "marketing_category": "ANDA", "marketing_start_date": "20110926", "listing_expiration_date": "20261231"}