diazepam

Generic: diazepam

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name diazepam
Generic Name diazepam
Labeler american health packaging
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

diazepam 5 mg/5mL

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-755
Product ID 60687-755_0293429b-79eb-fa1a-e063-6394a90a21cb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070928
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2023-07-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687755
Hyphenated Format 60687-755

Supplemental Identifiers

RxCUI
309843
UNII
Q3JTX2Q7TU
NUI
N0000175694 M0002356

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 ANDA070928 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/5mL
source: ndc
Packaging
  • 3 TRAY in 1 CASE (60687-755-86) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-755-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-755-40)
source: ndc

Packages (1)

Ingredients (1)

diazepam (5 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0293429b-79eb-fa1a-e063-6394a90a21cb", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["309843"], "spl_set_id": ["aeadf0b0-918b-40e0-a5e8-60b2fcbd5ded"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "3 TRAY in 1 CASE (60687-755-86)  / 10 CUP, UNIT-DOSE in 1 TRAY (60687-755-46)  / 5 mL in 1 CUP, UNIT-DOSE (60687-755-40)", "package_ndc": "60687-755-86", "marketing_start_date": "20230731"}], "brand_name": "Diazepam", "product_id": "60687-755_0293429b-79eb-fa1a-e063-6394a90a21cb", "dosage_form": "SOLUTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "60687-755", "dea_schedule": "CIV", "generic_name": "Diazepam", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "5 mg/5mL"}], "application_number": "ANDA070928", "marketing_category": "ANDA", "marketing_start_date": "20230731", "listing_expiration_date": "20261231"}