diazepam

Generic: diazepam

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

Drug Facts

Product Profile

Brand Name diazepam
Generic Name diazepam
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

diazepam 5 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-787
Product ID 62135-787_178ca1de-fc5d-991b-e063-6294a90a2570
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070303
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 1985-12-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135787
Hyphenated Format 62135-787

Supplemental Identifiers

RxCUI
197589 197590 197591
UPC
0362135788902 0362135787905 0362135786908
UNII
Q3JTX2Q7TU
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 diazepam (source: ndc)
Generic Name diazepam (source: ndc)
Application Number ANDA070303 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (62135-787-90)
source: ndc

Packages (1)

Ingredients (1)

diazepam (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "178ca1de-fc5d-991b-e063-6294a90a2570", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0362135788902", "0362135787905", "0362135786908"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197589", "197590", "197591"], "spl_set_id": ["6cb19468-be02-4219-9e80-94a28e2317b9"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-787-90)", "package_ndc": "62135-787-90", "marketing_start_date": "20240501"}], "brand_name": "Diazepam", "product_id": "62135-787_178ca1de-fc5d-991b-e063-6294a90a2570", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "62135-787", "dea_schedule": "CIV", "generic_name": "Diazepam", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "5 mg/1"}], "application_number": "ANDA070303", "marketing_category": "ANDA", "marketing_start_date": "19851220", "listing_expiration_date": "20261231"}