lorazepam

Generic: lorazepam

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lorazepam
Generic Name lorazepam
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lorazepam .5 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-228
Product ID 71205-228_08a911c9-3b1b-4404-a770-5bf4d27c7e96
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203572
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2017-03-24

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205228
Hyphenated Format 71205-228

Supplemental Identifiers

RxCUI
197900
UPC
0371205228309
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
  • .5 mg/1
source: ndc
Packaging
  • 2 TABLET in 1 BOTTLE (71205-228-02)
  • 3 TABLET in 1 BOTTLE (71205-228-03)
  • 15 TABLET in 1 BOTTLE (71205-228-15)
  • 20 TABLET in 1 BOTTLE (71205-228-20)
  • 30 TABLET in 1 BOTTLE (71205-228-30)
  • 60 TABLET in 1 BOTTLE (71205-228-60)
  • 90 TABLET in 1 BOTTLE (71205-228-90)
source: ndc

Packages (7)

71205-228-02 2 TABLET in 1 BOTTLE (71205-228-02) 71205-228-03 3 TABLET in 1 BOTTLE (71205-228-03) 71205-228-15 15 TABLET in 1 BOTTLE (71205-228-15) 71205-228-20 20 TABLET in 1 BOTTLE (71205-228-20) 71205-228-30 30 TABLET in 1 BOTTLE (71205-228-30) 71205-228-60 60 TABLET in 1 BOTTLE (71205-228-60) 71205-228-90 90 TABLET in 1 BOTTLE (71205-228-90)

Ingredients (1)

lorazepam (.5 mg/1)

Linked Drug Pages (1)

Lorazepam ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "08a911c9-3b1b-4404-a770-5bf4d27c7e96", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0371205228309"], "unii": ["O26FZP769L"], "rxcui": ["197900"], "spl_set_id": ["5b78f7af-0ad8-4fa1-a8c0-9308fe8d9b3a"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET in 1 BOTTLE (71205-228-02)", "package_ndc": "71205-228-02", "marketing_start_date": "20190201"}, {"sample": false, "description": "3 TABLET in 1 BOTTLE (71205-228-03)", "package_ndc": "71205-228-03", "marketing_start_date": "20190201"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71205-228-15)", "package_ndc": "71205-228-15", "marketing_start_date": "20210813"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71205-228-20)", "package_ndc": "71205-228-20", "marketing_start_date": "20190201"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-228-30)", "package_ndc": "71205-228-30", "marketing_start_date": "20190201"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-228-60)", "package_ndc": "71205-228-60", "marketing_start_date": "20190201"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-228-90)", "package_ndc": "71205-228-90", "marketing_start_date": "20190201"}], "brand_name": "Lorazepam", "product_id": "71205-228_08a911c9-3b1b-4404-a770-5bf4d27c7e96", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "71205-228", "dea_schedule": "CIV", "generic_name": "Lorazepam", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lorazepam", "active_ingredients": [{"name": "LORAZEPAM", "strength": ".5 mg/1"}], "application_number": "ANDA203572", "marketing_category": "ANDA", "marketing_start_date": "20170324", "listing_expiration_date": "20261231"}