loxapine
Generic: loxapine
Labeler: lannett company, inc.Drug Facts
Product Profile
Brand Name
loxapine
Generic Name
loxapine
Labeler
lannett company, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
loxapine succinate 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0527-1395
Product ID
0527-1395_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
05271395
Hyphenated Format
0527-1395
Supplemental Identifiers
RxCUI
UPC
UNII
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
loxapine (source: ndc)
Generic Name
loxapine (source: ndc)
Application Number
ANDA090695 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE, PLASTIC (0527-1395-01)
- 1000 CAPSULE in 1 BOTTLE, PLASTIC (0527-1395-10)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
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 (0527-1395-01)", "package_ndc": "0527-1395-01", "marketing_start_date": "20110926"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE, PLASTIC (0527-1395-10)", "package_ndc": "0527-1395-10", "marketing_start_date": "20110926"}], "brand_name": "Loxapine", "product_id": "0527-1395_d237714b-55f8-4a6e-9297-c10d41ab3cd2", "dosage_form": "CAPSULE", "product_ndc": "0527-1395", "generic_name": "Loxapine", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Loxapine", "active_ingredients": [{"name": "LOXAPINE SUCCINATE", "strength": "10 mg/1"}], "application_number": "ANDA090695", "marketing_category": "ANDA", "marketing_start_date": "20110926", "listing_expiration_date": "20261231"}