alprazolam

Generic: alprazolam

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

Drug Facts

Product Profile

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

alprazolam 1 mg/1

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 70954-510
Product ID 70954-510_18a6f29f-7eb8-4aa2-8121-d554c59da191
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074174
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2021-05-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70954510
Hyphenated Format 70954-510

Supplemental Identifiers

RxCUI
197321 197322 308047 308048
UPC
0370954508205 0370954509301 0370954510208 0370954511106 0370954508304 0370954508106 0370954509103 0370954510307 0370954510109 0370954511205 0370954509202
UNII
YU55MQ3IZY
NUI
N0000175694 M0002356

Packaging Origin

Original Packager
true

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 ANDA074174 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70954-510-10)
  • 500 TABLET in 1 BOTTLE (70954-510-20)
  • 1000 TABLET in 1 BOTTLE (70954-510-30)
source: ndc

Packages (3)

70954-510-10 100 TABLET in 1 BOTTLE (70954-510-10) 70954-510-20 500 TABLET in 1 BOTTLE (70954-510-20) 70954-510-30 1000 TABLET in 1 BOTTLE (70954-510-30)

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": "18a6f29f-7eb8-4aa2-8121-d554c59da191", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0370954508205", "0370954509301", "0370954510208", "0370954511106", "0370954508304", "0370954508106", "0370954509103", "0370954510307", "0370954510109", "0370954511205", "0370954509202"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321", "197322", "308047", "308048"], "spl_set_id": ["38428a1b-718c-49cc-94ae-2e3644ba6256"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70954-510-10)", "package_ndc": "70954-510-10", "marketing_start_date": "20210511"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70954-510-20)", "package_ndc": "70954-510-20", "marketing_start_date": "20210511"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (70954-510-30)", "package_ndc": "70954-510-30", "marketing_start_date": "20210511"}], "brand_name": "Alprazolam", "product_id": "70954-510_18a6f29f-7eb8-4aa2-8121-d554c59da191", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "70954-510", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": "1 mg/1"}], "application_number": "ANDA074174", "marketing_category": "ANDA", "marketing_start_date": "20210511", "listing_expiration_date": "20261231"}