loxapine

Generic: loxapine

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name loxapine
Generic Name loxapine
Labeler remedyrepack inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

loxapine succinate 50 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-0416
Product ID 70518-0416_4b1a1631-5210-3d55-e063-6294a90a03dc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072062
Listing Expiration 2027-12-31
Marketing Start 2017-04-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705180416
Hyphenated Format 70518-0416

Supplemental Identifiers

RxCUI
314075
UNII
X59SG0MRYU

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
  • 30 CAPSULE in 1 BLISTER PACK (70518-0416-0)
source: ndc

Packages (1)

70518-0416-0 30 CAPSULE in 1 BLISTER PACK (70518-0416-0)

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": "4b1a1631-5210-3d55-e063-6294a90a03dc", "openfda": {"unii": ["X59SG0MRYU"], "rxcui": ["314075"], "spl_set_id": ["ae8e299c-4003-4ccf-badc-fb665a997b20"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-0416-0)", "package_ndc": "70518-0416-0", "marketing_start_date": "20170410"}], "brand_name": "Loxapine", "product_id": "70518-0416_4b1a1631-5210-3d55-e063-6294a90a03dc", "dosage_form": "CAPSULE", "product_ndc": "70518-0416", "generic_name": "Loxapine", "labeler_name": "REMEDYREPACK 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": "20170410", "listing_expiration_date": "20271231"}