eletriptan hydrobromide
Generic: eletriptan hydrobromide
Labeler: teva pharmaceuticals usa, inc.Drug Facts
Product Profile
Brand Name
eletriptan hydrobromide
Generic Name
eletriptan hydrobromide
Labeler
teva pharmaceuticals usa, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
eletriptan hydrobromide 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0093-8310
Product ID
0093-8310_fe826d95-af0c-490d-8a5d-02218c836ff8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202040
Listing Expiration
2026-12-31
Marketing Start
2017-07-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00938310
Hyphenated Format
0093-8310
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
eletriptan hydrobromide (source: ndc)
Generic Name
eletriptan hydrobromide (source: ndc)
Application Number
ANDA202040 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 6 BLISTER PACK in 1 CARTON (0093-8310-18) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-8310-19)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fe826d95-af0c-490d-8a5d-02218c836ff8", "openfda": {"unii": ["M41W832TA3"], "rxcui": ["359493", "359494"], "spl_set_id": ["62dc12ce-4f19-41c6-9593-3cae29f04af1"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 BLISTER PACK in 1 CARTON (0093-8310-18) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-8310-19)", "package_ndc": "0093-8310-18", "marketing_start_date": "20170721"}], "brand_name": "Eletriptan Hydrobromide", "product_id": "0093-8310_fe826d95-af0c-490d-8a5d-02218c836ff8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "0093-8310", "generic_name": "Eletriptan Hydrobromide", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Eletriptan Hydrobromide", "active_ingredients": [{"name": "ELETRIPTAN HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "ANDA202040", "marketing_category": "ANDA", "marketing_start_date": "20170721", "listing_expiration_date": "20261231"}