alprazolam

Generic: alprazolam

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

alprazolam 1 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-609
Product ID 43063-609_2f3aacb7-ebbb-e49e-e063-6394a90a9176
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074112
DEA Schedule civ
Marketing Start 1995-12-29
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 43063609
Hyphenated Format 43063-609

Supplemental Identifiers

RxCUI
197321
UPC
0343063609309
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
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-609-30)
  • 40 TABLET in 1 BOTTLE, PLASTIC (43063-609-40)
  • 60 TABLET in 1 BOTTLE, PLASTIC (43063-609-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (43063-609-90)
source: ndc

Packages (4)

43063-609-30 30 TABLET in 1 BOTTLE, PLASTIC (43063-609-30) 43063-609-40 40 TABLET in 1 BOTTLE, PLASTIC (43063-609-40) 43063-609-60 60 TABLET in 1 BOTTLE, PLASTIC (43063-609-60) 43063-609-90 90 TABLET in 1 BOTTLE, PLASTIC (43063-609-90)

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": "2f3aacb7-ebbb-e49e-e063-6394a90a9176", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0343063609309"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321"], "spl_set_id": ["0ffcdbab-17e4-4395-8155-5b6ad00be6c2"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-609-30)", "package_ndc": "43063-609-30", "marketing_end_date": "20270319", "marketing_start_date": "20151006"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE, PLASTIC (43063-609-40)", "package_ndc": "43063-609-40", "marketing_end_date": "20270319", "marketing_start_date": "20151019"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-609-60)", "package_ndc": "43063-609-60", "marketing_end_date": "20270319", "marketing_start_date": "20150903"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-609-90)", "package_ndc": "43063-609-90", "marketing_end_date": "20270319", "marketing_start_date": "20150903"}], "brand_name": "Alprazolam", "product_id": "43063-609_2f3aacb7-ebbb-e49e-e063-6394a90a9176", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "43063-609", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "PD-Rx Pharmaceuticals, 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": "19951229"}