pregabalin

Generic: pregabalin

Labeler: eskayef pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pregabalin
Generic Name pregabalin
Labeler eskayef pharmaceuticals limited
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

pregabalin 75 mg/1

Manufacturer
Eskayef Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 72658-0810
Product ID 72658-0810_4739c18b-9a48-41df-e063-6394a90a3589
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212988
DEA Schedule cv
Listing Expiration 2026-12-31
Marketing Start 2022-04-04

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 726580810
Hyphenated Format 72658-0810

Supplemental Identifiers

RxCUI
483438 483440 483442 483444 483446 483448 483450 577127
UPC
0372658080810 0372658080919 0372658081411 0372658081312 0372658081114 0372658081015 0372658084917 0372658081213
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 ANDA212988 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 60 CAPSULE in 1 BOTTLE (72658-0810-1)
  • 90 CAPSULE in 1 BOTTLE (72658-0810-2)
  • 6 BLISTER PACK in 1 CARTON (72658-0810-3) / 10 CAPSULE in 1 BLISTER PACK
  • 10 BLISTER PACK in 1 CARTON (72658-0810-5) / 10 CAPSULE in 1 BLISTER PACK
  • 500 CAPSULE in 1 BOTTLE (72658-0810-6)
source: ndc

Packages (5)

Ingredients (1)

pregabalin (75 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4739c18b-9a48-41df-e063-6394a90a3589", "openfda": {"upc": ["0372658080810", "0372658080919", "0372658081411", "0372658081312", "0372658081114", "0372658081015", "0372658084917", "0372658081213"], "unii": ["55JG375S6M"], "rxcui": ["483438", "483440", "483442", "483444", "483446", "483448", "483450", "577127"], "spl_set_id": ["65d9e751-61c2-4741-85c0-2526cfdc765c"], "manufacturer_name": ["Eskayef Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (72658-0810-1)", "package_ndc": "72658-0810-1", "marketing_start_date": "20220404"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72658-0810-2)", "package_ndc": "72658-0810-2", "marketing_start_date": "20220404"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (72658-0810-3)  / 10 CAPSULE in 1 BLISTER PACK", "package_ndc": "72658-0810-3", "marketing_start_date": "20220404"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (72658-0810-5)  / 10 CAPSULE in 1 BLISTER PACK", "package_ndc": "72658-0810-5", "marketing_start_date": "20220404"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (72658-0810-6)", "package_ndc": "72658-0810-6", "marketing_start_date": "20220404"}], "brand_name": "PREGABALIN", "product_id": "72658-0810_4739c18b-9a48-41df-e063-6394a90a3589", "dosage_form": "CAPSULE", "product_ndc": "72658-0810", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "Eskayef Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREGABALIN", "active_ingredients": [{"name": "PREGABALIN", "strength": "75 mg/1"}], "application_number": "ANDA212988", "marketing_category": "ANDA", "marketing_start_date": "20220404", "listing_expiration_date": "20261231"}