lorazepam

Generic: lorazepam

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lorazepam
Generic Name lorazepam
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lorazepam 2 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-339
Product ID 72789-339_4bbd73ca-5b7d-da52-e063-6394a90ad855
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203572
DEA Schedule civ
Listing Expiration 2027-12-31
Marketing Start 2021-02-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789339
Hyphenated Format 72789-339

Supplemental Identifiers

RxCUI
197902
UPC
0372789339306
UNII
O26FZP769L
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 lorazepam (source: ndc)
Generic Name lorazepam (source: ndc)
Application Number ANDA203572 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-339-30)
source: ndc

Packages (1)

Ingredients (1)

lorazepam (2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4bbd73ca-5b7d-da52-e063-6394a90ad855", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0372789339306"], "unii": ["O26FZP769L"], "rxcui": ["197902"], "spl_set_id": ["0418ad09-3069-4381-9a8f-e41b234fdac6"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-339-30)", "package_ndc": "72789-339-30", "marketing_start_date": "20230727"}], "brand_name": "LORAZEPAM", "product_id": "72789-339_4bbd73ca-5b7d-da52-e063-6394a90ad855", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72789-339", "dea_schedule": "CIV", "generic_name": "LORAZEPAM", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LORAZEPAM", "active_ingredients": [{"name": "LORAZEPAM", "strength": "2 mg/1"}], "application_number": "ANDA203572", "marketing_category": "ANDA", "marketing_start_date": "20210201", "listing_expiration_date": "20271231"}