rabeprazole sodium

Generic: rabeprazole sodium

Labeler: ascend laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name rabeprazole sodium
Generic Name rabeprazole sodium
Labeler ascend laboratories, llc
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

rabeprazole sodium 20 mg/1

Manufacturer
Ascend Laboratories, LLC

Identifiers & Regulatory

Product NDC 67877-443
Product ID 67877-443_f3b11232-76f6-4cfd-84ac-73df3fa0d3a4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208644
Listing Expiration 2026-12-31
Marketing Start 2018-04-27

Pharmacologic Class

Classes
proton pump inhibitor [epc] proton pump inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67877443
Hyphenated Format 67877-443

Supplemental Identifiers

RxCUI
854868
UPC
0367877443904 0367877443300
UNII
3L36P16U4R

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 rabeprazole sodium (source: ndc)
Generic Name rabeprazole sodium (source: ndc)
Application Number ANDA208644 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (67877-443-30)
  • 100 POUCH in 1 CARTON (67877-443-38) / 1 BLISTER PACK in 1 POUCH / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67877-443-33)
  • 90 TABLET, DELAYED RELEASE in 1 BOTTLE (67877-443-90)
source: ndc

Packages (3)

67877-443-30 30 TABLET, DELAYED RELEASE in 1 BOTTLE (67877-443-30) 67877-443-38 100 POUCH in 1 CARTON (67877-443-38) / 1 BLISTER PACK in 1 POUCH / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67877-443-33) 67877-443-90 90 TABLET, DELAYED RELEASE in 1 BOTTLE (67877-443-90)

Ingredients (1)

rabeprazole sodium (20 mg/1)

Linked Drug Pages (1)

Rabeprazole Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f3b11232-76f6-4cfd-84ac-73df3fa0d3a4", "openfda": {"upc": ["0367877443904", "0367877443300"], "unii": ["3L36P16U4R"], "rxcui": ["854868"], "spl_set_id": ["45092108-7c4a-48f9-8222-ca8612e82189"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (67877-443-30)", "package_ndc": "67877-443-30", "marketing_start_date": "20180427"}, {"sample": false, "description": "100 POUCH in 1 CARTON (67877-443-38)  / 1 BLISTER PACK in 1 POUCH / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67877-443-33)", "package_ndc": "67877-443-38", "marketing_start_date": "20180427"}, {"sample": false, "description": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (67877-443-90)", "package_ndc": "67877-443-90", "marketing_start_date": "20180427"}], "brand_name": "Rabeprazole Sodium", "product_id": "67877-443_f3b11232-76f6-4cfd-84ac-73df3fa0d3a4", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "67877-443", "generic_name": "Rabeprazole Sodium", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rabeprazole Sodium", "active_ingredients": [{"name": "RABEPRAZOLE SODIUM", "strength": "20 mg/1"}], "application_number": "ANDA208644", "marketing_category": "ANDA", "marketing_start_date": "20180427", "listing_expiration_date": "20261231"}