alprazolam
Generic: alprazolam
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
alprazolam
Generic Name
alprazolam
Labeler
american health packaging
Dosage Form
TABLET
Routes
Active Ingredients
alprazolam .25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-377
Product ID
60687-377_2a81392c-12be-e4aa-e063-6394a90a3d45
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203346
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2023-11-09
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687377
Hyphenated Format
60687-377
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
- .25 mg/1
Packaging
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-377-01) / 1 TABLET in 1 BLISTER PACK (60687-377-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a81392c-12be-e4aa-e063-6394a90a3d45", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["308047", "308048"], "spl_set_id": ["ea95d182-453b-4c43-8402-d65c488d55f2"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-377-01) / 1 TABLET in 1 BLISTER PACK (60687-377-11)", "package_ndc": "60687-377-01", "marketing_start_date": "20231109"}], "brand_name": "Alprazolam", "product_id": "60687-377_2a81392c-12be-e4aa-e063-6394a90a3d45", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "60687-377", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".25 mg/1"}], "application_number": "ANDA203346", "marketing_category": "ANDA", "marketing_start_date": "20231109", "listing_expiration_date": "20261231"}