pregabalin

Generic: pregabalin

Labeler: novadoz pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pregabalin
Generic Name pregabalin
Labeler novadoz pharmaceuticals llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

pregabalin 25 mg/1

Manufacturer
Novadoz Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72205-011
Product ID 72205-011_d1428cf2-1243-43cb-8b54-f46024dbca29
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209357
DEA Schedule cv
Listing Expiration 2026-12-31
Marketing Start 2019-07-19

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72205011
Hyphenated Format 72205-011

Supplemental Identifiers

RxCUI
483438 483440 483442 483444 483446 483448 483450 577127
UPC
0372205012905 0372205017900 0372205011908 0372205015906 0372205014909 0372205013902 0372205016903 0372205018907
UNII
55JG375S6M

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 pregabalin (source: ndc)
Generic Name pregabalin (source: ndc)
Application Number ANDA209357 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (72205-011-06) / 10 CAPSULE in 1 BLISTER PACK (72205-011-11)
  • 90 CAPSULE in 1 BOTTLE (72205-011-90)
  • 1000 CAPSULE in 1 BOTTLE (72205-011-99)
source: ndc

Packages (3)

72205-011-06 100 BLISTER PACK in 1 CARTON (72205-011-06) / 10 CAPSULE in 1 BLISTER PACK (72205-011-11) 72205-011-90 90 CAPSULE in 1 BOTTLE (72205-011-90) 72205-011-99 1000 CAPSULE in 1 BOTTLE (72205-011-99)

Ingredients (1)

pregabalin (25 mg/1)

Linked Drug Pages (1)

Pregabalin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d1428cf2-1243-43cb-8b54-f46024dbca29", "openfda": {"upc": ["0372205012905", "0372205017900", "0372205011908", "0372205015906", "0372205014909", "0372205013902", "0372205016903", "0372205018907"], "unii": ["55JG375S6M"], "rxcui": ["483438", "483440", "483442", "483444", "483446", "483448", "483450", "577127"], "spl_set_id": ["193666f7-3c55-43b1-947a-2ffec40c687f"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (72205-011-06)  / 10 CAPSULE in 1 BLISTER PACK (72205-011-11)", "package_ndc": "72205-011-06", "marketing_start_date": "20190719"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72205-011-90)", "package_ndc": "72205-011-90", "marketing_start_date": "20190719"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (72205-011-99)", "package_ndc": "72205-011-99", "marketing_start_date": "20190719"}], "brand_name": "Pregabalin", "product_id": "72205-011_d1428cf2-1243-43cb-8b54-f46024dbca29", "dosage_form": "CAPSULE", "product_ndc": "72205-011", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "25 mg/1"}], "application_number": "ANDA209357", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}