flurazepam hydrochloride

Generic: flurazepam hydrochloride

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name flurazepam hydrochloride
Generic Name flurazepam hydrochloride
Labeler chartwell rx, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

flurazepam hydrochloride 30 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-737
Product ID 62135-737_25893c92-c8f1-567a-e063-6294a90a00d4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072369
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 1989-03-30

Pharmacologic Class

Classes
benzodiazepine [epc] benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135737
Hyphenated Format 62135-737

Supplemental Identifiers

RxCUI
1298088 1298091
UPC
0362135736309 0362135736903 0362135737306 0362135737900
UNII
756RDM536M

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 flurazepam hydrochloride (source: ndc)
Generic Name flurazepam hydrochloride (source: ndc)
Application Number ANDA072369 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (62135-737-30)
  • 90 CAPSULE in 1 BOTTLE (62135-737-90)
source: ndc

Packages (2)

Ingredients (1)

flurazepam hydrochloride (30 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "25893c92-c8f1-567a-e063-6294a90a00d4", "openfda": {"upc": ["0362135736309", "0362135736903", "0362135737306", "0362135737900"], "unii": ["756RDM536M"], "rxcui": ["1298088", "1298091"], "spl_set_id": ["8f476891-1346-4e8c-ac1b-f8cbdc64f5a1"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (62135-737-30)", "package_ndc": "62135-737-30", "marketing_start_date": "20231219"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (62135-737-90)", "package_ndc": "62135-737-90", "marketing_start_date": "20230908"}], "brand_name": "Flurazepam Hydrochloride", "product_id": "62135-737_25893c92-c8f1-567a-e063-6294a90a00d4", "dosage_form": "CAPSULE", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "62135-737", "dea_schedule": "CIV", "generic_name": "Flurazepam Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Flurazepam Hydrochloride", "active_ingredients": [{"name": "FLURAZEPAM HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA072369", "marketing_category": "ANDA", "marketing_start_date": "19890330", "listing_expiration_date": "20261231"}