mycapssa

Generic: octreotide

Labeler: amryt pharmaceuticals designated activity company
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name mycapssa
Generic Name octreotide
Labeler amryt pharmaceuticals designated activity company
Dosage Form CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

octreotide 20 mg/1

Manufacturer
Amryt Pharmaceuticals Designated Activity Company

Identifiers & Regulatory

Product NDC 69880-120
Product ID 69880-120_1f0f9540-123a-49d7-b1d2-0c150dd5f26a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA208232
Listing Expiration 2026-12-31
Marketing Start 2020-07-06

Pharmacologic Class

Established (EPC)
somatostatin analog [epc]
Mechanism of Action
somatostatin receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69880120
Hyphenated Format 69880-120

Supplemental Identifiers

RxCUI
2380611 2380617
UNII
RWM8CCW8GP
NUI
N0000175904 N0000000194

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 mycapssa (source: ndc)
Generic Name octreotide (source: ndc)
Application Number NDA208232 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 4 BLISTER PACK in 1 DOSE PACK (69880-120-28) / 7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

octreotide (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1f0f9540-123a-49d7-b1d2-0c150dd5f26a", "openfda": {"nui": ["N0000175904", "N0000000194"], "unii": ["RWM8CCW8GP"], "rxcui": ["2380611", "2380617"], "spl_set_id": ["62a5e1eb-b48e-4ea6-8781-f75e490b17e4"], "pharm_class_epc": ["Somatostatin Analog [EPC]"], "pharm_class_moa": ["Somatostatin Receptor Agonists [MoA]"], "manufacturer_name": ["Amryt Pharmaceuticals Designated Activity Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 DOSE PACK (69880-120-28)  / 7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "69880-120-28", "marketing_start_date": "20200706"}], "brand_name": "Mycapssa", "product_id": "69880-120_1f0f9540-123a-49d7-b1d2-0c150dd5f26a", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Somatostatin Analog [EPC]", "Somatostatin Receptor Agonists [MoA]"], "product_ndc": "69880-120", "generic_name": "Octreotide", "labeler_name": "Amryt Pharmaceuticals Designated Activity Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mycapssa", "active_ingredients": [{"name": "OCTREOTIDE", "strength": "20 mg/1"}], "application_number": "NDA208232", "marketing_category": "NDA", "marketing_start_date": "20200706", "listing_expiration_date": "20261231"}