lorazepam
Generic: lorazepam
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
lorazepam
Generic Name
lorazepam
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
lorazepam .5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-0329
Product ID
71335-0329_1577a3f6-8289-4621-a0e5-9d69bc6218d3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078203
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2023-05-16
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713350329
Hyphenated Format
71335-0329
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA078203 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (71335-0329-1)
- 10 TABLET in 1 BOTTLE (71335-0329-2)
- 60 TABLET in 1 BOTTLE (71335-0329-3)
- 90 TABLET in 1 BOTTLE (71335-0329-4)
- 15 TABLET in 1 BOTTLE (71335-0329-5)
- 100 TABLET in 1 BOTTLE (71335-0329-6)
- 120 TABLET in 1 BOTTLE (71335-0329-7)
- 2 TABLET in 1 BOTTLE (71335-0329-8)
- 5 TABLET in 1 BOTTLE (71335-0329-9)
Packages (9)
71335-0329-1
30 TABLET in 1 BOTTLE (71335-0329-1)
71335-0329-2
10 TABLET in 1 BOTTLE (71335-0329-2)
71335-0329-3
60 TABLET in 1 BOTTLE (71335-0329-3)
71335-0329-4
90 TABLET in 1 BOTTLE (71335-0329-4)
71335-0329-5
15 TABLET in 1 BOTTLE (71335-0329-5)
71335-0329-6
100 TABLET in 1 BOTTLE (71335-0329-6)
71335-0329-7
120 TABLET in 1 BOTTLE (71335-0329-7)
71335-0329-8
2 TABLET in 1 BOTTLE (71335-0329-8)
71335-0329-9
5 TABLET in 1 BOTTLE (71335-0329-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1577a3f6-8289-4621-a0e5-9d69bc6218d3", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["O26FZP769L"], "rxcui": ["197900"], "spl_set_id": ["aac672f9-0ba7-4852-b8a7-caac9e4b1e77"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0329-1)", "package_ndc": "71335-0329-1", "marketing_start_date": "20240515"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-0329-2)", "package_ndc": "71335-0329-2", "marketing_start_date": "20240515"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0329-3)", "package_ndc": "71335-0329-3", "marketing_start_date": "20240515"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0329-4)", "package_ndc": "71335-0329-4", "marketing_start_date": "20240515"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-0329-5)", "package_ndc": "71335-0329-5", "marketing_start_date": "20240515"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-0329-6)", "package_ndc": "71335-0329-6", "marketing_start_date": "20240515"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-0329-7)", "package_ndc": "71335-0329-7", "marketing_start_date": "20240515"}, {"sample": false, "description": "2 TABLET in 1 BOTTLE (71335-0329-8)", "package_ndc": "71335-0329-8", "marketing_start_date": "20240515"}, {"sample": false, "description": "5 TABLET in 1 BOTTLE (71335-0329-9)", "package_ndc": "71335-0329-9", "marketing_start_date": "20240515"}], "brand_name": "Lorazepam", "product_id": "71335-0329_1577a3f6-8289-4621-a0e5-9d69bc6218d3", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "71335-0329", "dea_schedule": "CIV", "generic_name": "Lorazepam", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lorazepam", "active_ingredients": [{"name": "LORAZEPAM", "strength": ".5 mg/1"}], "application_number": "ANDA078203", "marketing_category": "ANDA", "marketing_start_date": "20230516", "listing_expiration_date": "20261231"}