alprazolam
Generic: alprazolam
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
alprazolam
Generic Name
alprazolam
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
alprazolam .5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-9666
Product ID
71335-9666_23cf41d9-0bbc-4bbc-8436-db45b75c1d73
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)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713359666
Hyphenated Format
71335-9666
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
alprazolam (source: ndc)
Generic Name
alprazolam (source: ndc)
Application Number
ANDA203346 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 mg/1
Packaging
- 10 TABLET in 1 BOTTLE (71335-9666-0)
- 15 TABLET in 1 BOTTLE (71335-9666-1)
- 30 TABLET in 1 BOTTLE (71335-9666-2)
- 20 TABLET in 1 BOTTLE (71335-9666-3)
- 100 TABLET in 1 BOTTLE (71335-9666-4)
- 90 TABLET in 1 BOTTLE (71335-9666-5)
- 60 TABLET in 1 BOTTLE (71335-9666-6)
- 120 TABLET in 1 BOTTLE (71335-9666-7)
- 28 TABLET in 1 BOTTLE (71335-9666-8)
- 2 TABLET in 1 BOTTLE (71335-9666-9)
Packages (10)
71335-9666-0
10 TABLET in 1 BOTTLE (71335-9666-0)
71335-9666-1
15 TABLET in 1 BOTTLE (71335-9666-1)
71335-9666-2
30 TABLET in 1 BOTTLE (71335-9666-2)
71335-9666-3
20 TABLET in 1 BOTTLE (71335-9666-3)
71335-9666-4
100 TABLET in 1 BOTTLE (71335-9666-4)
71335-9666-5
90 TABLET in 1 BOTTLE (71335-9666-5)
71335-9666-6
60 TABLET in 1 BOTTLE (71335-9666-6)
71335-9666-7
120 TABLET in 1 BOTTLE (71335-9666-7)
71335-9666-8
28 TABLET in 1 BOTTLE (71335-9666-8)
71335-9666-9
2 TABLET in 1 BOTTLE (71335-9666-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "23cf41d9-0bbc-4bbc-8436-db45b75c1d73", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["308048"], "spl_set_id": ["2bd0d4c6-0fde-46f2-bb13-da25d50427df"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-9666-0)", "package_ndc": "71335-9666-0", "marketing_start_date": "20230327"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-9666-1)", "package_ndc": "71335-9666-1", "marketing_start_date": "20230327"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-9666-2)", "package_ndc": "71335-9666-2", "marketing_start_date": "20230327"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-9666-3)", "package_ndc": "71335-9666-3", "marketing_start_date": "20230327"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-9666-4)", "package_ndc": "71335-9666-4", "marketing_start_date": "20230327"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-9666-5)", "package_ndc": "71335-9666-5", "marketing_start_date": "20230327"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-9666-6)", "package_ndc": "71335-9666-6", "marketing_start_date": "20230327"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-9666-7)", "package_ndc": "71335-9666-7", "marketing_start_date": "20230327"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-9666-8)", "package_ndc": "71335-9666-8", "marketing_start_date": "20230327"}, {"sample": false, "description": "2 TABLET in 1 BOTTLE (71335-9666-9)", "package_ndc": "71335-9666-9", "marketing_start_date": "20230327"}], "brand_name": "Alprazolam", "product_id": "71335-9666_23cf41d9-0bbc-4bbc-8436-db45b75c1d73", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "71335-9666", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "Bryant Ranch Prepack", "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"}