quazepam

Generic: quazepam

Labeler: atland pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name quazepam
Generic Name quazepam
Labeler atland pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

quazepam 15 mg/1

Manufacturer
Atland Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 71993-265
Product ID 71993-265_41da82ab-fab6-7eba-e063-6394a90a037e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA018708
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2018-03-20

Pharmacologic Class

Established (EPC)
benzodiazepine [epc]
Chemical Structure
benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71993265
Hyphenated Format 71993-265

Supplemental Identifiers

RxCUI
198183
UPC
0371993265302
UNII
JF8V0828ZI
NUI
N0000175694 M0002356

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 quazepam (source: ndc)
Generic Name quazepam (source: ndc)
Application Number NDA018708 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71993-265-30)
source: ndc

Packages (1)

71993-265-30 30 TABLET in 1 BOTTLE (71993-265-30)

Ingredients (1)

quazepam (15 mg/1)

Linked Drug Pages (1)

Quazepam ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "41da82ab-fab6-7eba-e063-6394a90a037e", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0371993265302"], "unii": ["JF8V0828ZI"], "rxcui": ["198183"], "spl_set_id": ["f7d63f3f-5303-48ab-bce2-35fd62c45799"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Atland Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71993-265-30)", "package_ndc": "71993-265-30", "marketing_start_date": "20180320"}], "brand_name": "Quazepam", "product_id": "71993-265_41da82ab-fab6-7eba-e063-6394a90a037e", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "71993-265", "dea_schedule": "CIV", "generic_name": "Quazepam", "labeler_name": "Atland Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Quazepam", "active_ingredients": [{"name": "QUAZEPAM", "strength": "15 mg/1"}], "application_number": "NDA018708", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20180320", "listing_expiration_date": "20261231"}