sucralfate

Generic: sucralfate

Labeler: strides pharma science limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sucralfate
Generic Name sucralfate
Labeler strides pharma science limited
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

sucralfate 1 g/10mL

Manufacturer
Strides Pharma Science Limited

Identifiers & Regulatory

Product NDC 64380-149
Product ID 64380-149_06c3071e-36b7-4d88-aaa8-2010a3358042
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216474
Listing Expiration 2026-12-31
Marketing Start 2024-07-10

Pharmacologic Class

Established (EPC)
aluminum complex [epc]
Chemical Structure
organometallic compounds [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 64380149
Hyphenated Format 64380-149

Supplemental Identifiers

RxCUI
313123
UPC
0364380149019
UNII
XX73205DH5
NUI
N0000175801 M0015420

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 sucralfate (source: ndc)
Generic Name sucralfate (source: ndc)
Application Number ANDA216474 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/10mL
source: ndc
Packaging
  • 420 mL in 1 BOTTLE, PLASTIC (64380-149-01)
  • 5 CUP, UNIT-DOSE in 1 TRAY (64380-149-03) / 10 mL in 1 CUP, UNIT-DOSE (64380-149-02)
  • 3 TRAY in 1 CARTON (64380-149-04) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (64380-149-02)
  • 4 TRAY in 1 CARTON (64380-149-05) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (64380-149-02)
  • 5 TRAY in 1 CARTON (64380-149-06) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (64380-149-02)
  • 10 TRAY in 1 CARTON (64380-149-07) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (64380-149-02)
source: ndc

Packages (6)

Ingredients (1)

sucralfate (1 g/10mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "06c3071e-36b7-4d88-aaa8-2010a3358042", "openfda": {"nui": ["N0000175801", "M0015420"], "upc": ["0364380149019"], "unii": ["XX73205DH5"], "rxcui": ["313123"], "spl_set_id": ["8e25bff2-769e-4bd4-a6de-895c58b840d2"], "pharm_class_cs": ["Organometallic Compounds [CS]"], "pharm_class_epc": ["Aluminum Complex [EPC]"], "manufacturer_name": ["Strides Pharma Science Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "420 mL in 1 BOTTLE, PLASTIC (64380-149-01)", "package_ndc": "64380-149-01", "marketing_start_date": "20240710"}, {"sample": false, "description": "5 CUP, UNIT-DOSE in 1 TRAY (64380-149-03)  / 10 mL in 1 CUP, UNIT-DOSE (64380-149-02)", "package_ndc": "64380-149-03", "marketing_start_date": "20240710"}, {"sample": false, "description": "3 TRAY in 1 CARTON (64380-149-04)  / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (64380-149-02)", "package_ndc": "64380-149-04", "marketing_start_date": "20240710"}, {"sample": false, "description": "4 TRAY in 1 CARTON (64380-149-05)  / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (64380-149-02)", "package_ndc": "64380-149-05", "marketing_start_date": "20240710"}, {"sample": false, "description": "5 TRAY in 1 CARTON (64380-149-06)  / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (64380-149-02)", "package_ndc": "64380-149-06", "marketing_start_date": "20240710"}, {"sample": false, "description": "10 TRAY in 1 CARTON (64380-149-07)  / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (64380-149-02)", "package_ndc": "64380-149-07", "marketing_start_date": "20240710"}], "brand_name": "sucralfate", "product_id": "64380-149_06c3071e-36b7-4d88-aaa8-2010a3358042", "dosage_form": "SUSPENSION", "pharm_class": ["Aluminum Complex [EPC]", "Organometallic Compounds [CS]"], "product_ndc": "64380-149", "generic_name": "Sucralfate", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "sucralfate", "active_ingredients": [{"name": "SUCRALFATE", "strength": "1 g/10mL"}], "application_number": "ANDA216474", "marketing_category": "ANDA", "marketing_start_date": "20240710", "listing_expiration_date": "20261231"}