zaleplon
Generic: zaleplon
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
zaleplon
Generic Name
zaleplon
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
zaleplon 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43063-912
Product ID
43063-912_415d7fa5-73ac-93e7-e063-6294a90a02a3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077237
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2008-06-06
Pharmacologic Class
Established (EPC)
Mechanism of Action
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43063912
Hyphenated Format
43063-912
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
zaleplon (source: ndc)
Generic Name
zaleplon (source: ndc)
Application Number
ANDA077237 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 10 CAPSULE in 1 BOTTLE, PLASTIC (43063-912-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "415d7fa5-73ac-93e7-e063-6294a90a02a3", "openfda": {"nui": ["N0000183360", "N0000000196", "N0000175728"], "upc": ["0343063912102"], "unii": ["S62U433RMH"], "rxcui": ["313761"], "spl_set_id": ["a1277ef5-6072-43ff-a6ce-0a7cea58b7cb"], "pharm_class_pe": ["Central Nervous System Depression [PE]"], "pharm_class_epc": ["gamma-Aminobutyric Acid A Receptor Agonist [EPC]"], "pharm_class_moa": ["GABA A Agonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 CAPSULE in 1 BOTTLE, PLASTIC (43063-912-10)", "package_ndc": "43063-912-10", "marketing_start_date": "20181205"}], "brand_name": "Zaleplon", "product_id": "43063-912_415d7fa5-73ac-93e7-e063-6294a90a02a3", "dosage_form": "CAPSULE", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Agonists [MoA]", "gamma-Aminobutyric Acid A Receptor Agonist [EPC]"], "product_ndc": "43063-912", "dea_schedule": "CIV", "generic_name": "Zaleplon", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zaleplon", "active_ingredients": [{"name": "ZALEPLON", "strength": "10 mg/1"}], "application_number": "ANDA077237", "marketing_category": "ANDA", "marketing_start_date": "20080606", "listing_expiration_date": "20261231"}