pregabalin

Generic: pregabalin

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pregabalin
Generic Name pregabalin
Labeler proficient rx lp
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

pregabalin 150 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-188
Product ID 82804-188_efc36145-fffd-44de-9a42-f277d0ff39c9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206912
DEA Schedule cv
Listing Expiration 2026-12-31
Marketing Start 2019-10-08

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804188
Hyphenated Format 82804-188

Supplemental Identifiers

RxCUI
483440
UPC
0382804188604
UNII
55JG375S6M

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 ANDA206912 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 60 CAPSULE in 1 BOTTLE (82804-188-60)
source: ndc

Packages (1)

Ingredients (1)

pregabalin (150 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "efc36145-fffd-44de-9a42-f277d0ff39c9", "openfda": {"upc": ["0382804188604"], "unii": ["55JG375S6M"], "rxcui": ["483440"], "spl_set_id": ["efc36145-fffd-44de-9a42-f277d0ff39c9"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (82804-188-60)", "package_ndc": "82804-188-60", "marketing_start_date": "20250117"}], "brand_name": "Pregabalin", "product_id": "82804-188_efc36145-fffd-44de-9a42-f277d0ff39c9", "dosage_form": "CAPSULE", "product_ndc": "82804-188", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "150 mg/1"}], "application_number": "ANDA206912", "marketing_category": "ANDA", "marketing_start_date": "20191008", "listing_expiration_date": "20261231"}