alprazolam

Generic: alprazolam

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alprazolam
Generic Name alprazolam
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alprazolam .5 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3818
Product ID 68071-3818_315b8d50-f3b5-49a4-e063-6394a90ae849
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203346
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2015-07-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713818
Hyphenated Format 68071-3818

Supplemental Identifiers

RxCUI
308048
UPC
0368071381818
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 ANDA203346 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (68071-3818-1)
source: ndc

Packages (1)

68071-3818-1 1000 TABLET in 1 BOTTLE (68071-3818-1)

Ingredients (1)

alprazolam (.5 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": "315b8d50-f3b5-49a4-e063-6394a90ae849", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0368071381818"], "unii": ["YU55MQ3IZY"], "rxcui": ["308048"], "spl_set_id": ["315b8cf2-01a0-3f7d-e063-6394a90a39b5"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (68071-3818-1)", "package_ndc": "68071-3818-1", "marketing_start_date": "20250327"}], "brand_name": "Alprazolam", "product_id": "68071-3818_315b8d50-f3b5-49a4-e063-6394a90ae849", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "68071-3818", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".5 mg/1"}], "application_number": "ANDA203346", "marketing_category": "ANDA", "marketing_start_date": "20150731", "listing_expiration_date": "20261231"}