pregabalin

Generic: pregabalin

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pregabalin
Generic Name pregabalin
Labeler northstar rxllc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

pregabalin 200 mg/1

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 72603-357
Product ID 72603-357_45bca2c9-2de2-8684-e063-6294a90a1bdd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206912
DEA Schedule cv
Listing Expiration 2026-12-31
Marketing Start 2025-12-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603357
Hyphenated Format 72603-357

Supplemental Identifiers

RxCUI
483438 483440 483442 483444 483446 483448 483450
UPC
0372603357011 0372603353013 0372603358018 0372603352016 0372603355017 0372603356014 0372603354010
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 ANDA206912 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 90 CAPSULE in 1 BOTTLE (72603-357-01)
source: ndc

Packages (1)

Ingredients (1)

pregabalin (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45bca2c9-2de2-8684-e063-6294a90a1bdd", "openfda": {"upc": ["0372603357011", "0372603353013", "0372603358018", "0372603352016", "0372603355017", "0372603356014", "0372603354010"], "unii": ["55JG375S6M"], "rxcui": ["483438", "483440", "483442", "483444", "483446", "483448", "483450"], "spl_set_id": ["4a4d4c76-31c5-413b-be7c-82cb8091c19d"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72603-357-01)", "package_ndc": "72603-357-01", "marketing_start_date": "20251215"}], "brand_name": "Pregabalin", "product_id": "72603-357_45bca2c9-2de2-8684-e063-6294a90a1bdd", "dosage_form": "CAPSULE", "product_ndc": "72603-357", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "200 mg/1"}], "application_number": "ANDA206912", "marketing_category": "ANDA", "marketing_start_date": "20251215", "listing_expiration_date": "20261231"}