alprazolam

Generic: alprazolam

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

Drug Facts

Product Profile

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

alprazolam 1 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4137
Product ID 70518-4137_1cf8baf2-ee1d-a98b-e063-6394a90a0c81
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074112
DEA Schedule civ
Marketing Start 2024-07-10
Marketing End 2027-03-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184137
Hyphenated Format 70518-4137

Supplemental Identifiers

RxCUI
197321
UNII
YU55MQ3IZY
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 alprazolam (source: ndc)
Generic Name alprazolam (source: ndc)
Application Number ANDA074112 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE, PLASTIC (70518-4137-0)
source: ndc

Packages (1)

70518-4137-0 60 TABLET in 1 BOTTLE, PLASTIC (70518-4137-0)

Ingredients (1)

alprazolam (1 mg/1)

Linked Drug Pages (1)

Alprazolam ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1cf8baf2-ee1d-a98b-e063-6394a90a0c81", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321"], "spl_set_id": ["563e09db-2f3d-4ce8-b356-ae44477be6d0"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (70518-4137-0)", "package_ndc": "70518-4137-0", "marketing_end_date": "20270319", "marketing_start_date": "20240710"}], "brand_name": "Alprazolam", "product_id": "70518-4137_1cf8baf2-ee1d-a98b-e063-6394a90a0c81", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "70518-4137", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": "1 mg/1"}], "application_number": "ANDA074112", "marketing_category": "ANDA", "marketing_end_date": "20270319", "marketing_start_date": "20240710"}