lorazepam

Generic: lorazepam

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lorazepam
Generic Name lorazepam
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lorazepam 1 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2186
Product ID 70518-2186_38cb5e7e-0bdb-3d40-e063-6294a90a0d1b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078203
DEA Schedule civ
Marketing Start 2019-07-02
Marketing End 2026-08-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182186
Hyphenated Format 70518-2186

Supplemental Identifiers

RxCUI
197901
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 ANDA078203 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-2186-2)
source: ndc

Packages (1)

Ingredients (1)

lorazepam (1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38cb5e7e-0bdb-3d40-e063-6294a90a0d1b", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["O26FZP769L"], "rxcui": ["197901"], "spl_set_id": ["eb068a0f-5c0e-4218-b4c5-a0d0b1d362bd"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2186-2)", "package_ndc": "70518-2186-2", "marketing_end_date": "20260831", "marketing_start_date": "20240621"}], "brand_name": "Lorazepam", "product_id": "70518-2186_38cb5e7e-0bdb-3d40-e063-6294a90a0d1b", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "70518-2186", "dea_schedule": "CIV", "generic_name": "Lorazepam", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lorazepam", "active_ingredients": [{"name": "LORAZEPAM", "strength": "1 mg/1"}], "application_number": "ANDA078203", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20190702"}