sumatriptan succinate

Generic: sumatriptan succinate

Labeler: fresenius kabi usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sumatriptan succinate
Generic Name sumatriptan succinate
Labeler fresenius kabi usa, llc
Dosage Form INJECTION
Routes
SUBCUTANEOUS
Active Ingredients

sumatriptan succinate 6 mg/.5mL

Manufacturer
Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 63323-273
Product ID 63323-273_ae034e54-f171-44df-b13b-6eb588979001
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079242
Listing Expiration 2026-12-31
Marketing Start 2011-04-12

Pharmacologic Class

Classes
serotonin 1b receptor agonists [moa] serotonin 1d receptor agonists [moa] serotonin-1b and serotonin-1d receptor agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63323273
Hyphenated Format 63323-273

Supplemental Identifiers

RxCUI
313165
UPC
0363323273019
UNII
J8BDZ68989

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 sumatriptan succinate (source: ndc)
Generic Name sumatriptan succinate (source: ndc)
Application Number ANDA079242 (source: ndc)
Routes
SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 6 mg/.5mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (63323-273-01) / .5 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

63323-273-01 1 VIAL, SINGLE-DOSE in 1 CARTON (63323-273-01) / .5 mL in 1 VIAL, SINGLE-DOSE

Ingredients (1)

sumatriptan succinate (6 mg/.5mL)

Linked Drug Pages (1)

Sumatriptan Succinate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBCUTANEOUS"], "spl_id": "ae034e54-f171-44df-b13b-6eb588979001", "openfda": {"upc": ["0363323273019"], "unii": ["J8BDZ68989"], "rxcui": ["313165"], "spl_set_id": ["b183c7ba-2cc6-4854-a9a6-71ccd3592586"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (63323-273-01)  / .5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "63323-273-01", "marketing_start_date": "20110412"}], "brand_name": "Sumatriptan Succinate", "product_id": "63323-273_ae034e54-f171-44df-b13b-6eb588979001", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "63323-273", "generic_name": "Sumatriptan Succinate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan Succinate", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "6 mg/.5mL"}], "application_number": "ANDA079242", "marketing_category": "ANDA", "marketing_start_date": "20110412", "listing_expiration_date": "20261231"}