lorazepam
Generic: lorazepam
Labeler: direct rxDrug Facts
Product Profile
Brand Name
lorazepam
Generic Name
lorazepam
Labeler
direct rx
Dosage Form
TABLET
Routes
Active Ingredients
lorazepam .5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
61919-062
Product ID
61919-062_47e14ab4-5eb4-67c7-e063-6394a90a1e4b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078203
DEA Schedule
civ
Listing Expiration
2027-12-31
Marketing Start
2017-02-10
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
61919062
Hyphenated Format
61919-062
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
- 2 TABLET in 1 BOTTLE (61919-062-02)
- 60 TABLET in 1 BOTTLE (61919-062-60)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47e14ab4-5eb4-67c7-e063-6394a90a1e4b", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["O26FZP769L"], "rxcui": ["197900"], "spl_set_id": ["4832f02d-289c-2fe6-e054-00144ff8d46c"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET in 1 BOTTLE (61919-062-02)", "package_ndc": "61919-062-02", "marketing_start_date": "20170210"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (61919-062-60)", "package_ndc": "61919-062-60", "marketing_start_date": "20170210"}], "brand_name": "LORAZEPAM", "product_id": "61919-062_47e14ab4-5eb4-67c7-e063-6394a90a1e4b", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "61919-062", "dea_schedule": "CIV", "generic_name": "LORAZEPAM", "labeler_name": "DIRECT RX", "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": "20170210", "listing_expiration_date": "20271231"}