olanzapine (13668-171) | FunFoxMeds NDC

Drug Facts

Product Profile

Brand Name olanzapine

Generic Name olanzapine

Labeler torrent pharmaceuticals limited

Dosage Form TABLET

Routes

ORAL

Active Ingredients

olanzapine 20 mg/1

Manufacturer

Torrent Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 13668-171

Product ID 13668-171_1a64829a-2434-4c8d-8e58-9b28758e4b88

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA091434

Listing Expiration 2027-12-31

Marketing Start 2026-02-28

Pharmacologic Class

Established (EPC)

atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 13668171

Hyphenated Format 13668-171

Supplemental Identifiers

RxCUI

200034 283639 312076 312077 312078 312079 314154 314155 351107 351108

UPC

0313668088304 0313668170306 0313668169300 0313668171303 0313668168303 0313668166309 0313668090307 0313668089301 0313668167306 0313668086300

UNII

N7U69T4SZR

NUI

N0000175430

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 olanzapine (source: ndc)

Generic Name olanzapine (source: ndc)

Application Number ANDA091434 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

20 mg/1

source: ndc

Packaging

100 TABLET in 1 BOTTLE (13668-171-01)
500 TABLET in 1 BOTTLE (13668-171-05)
1000 TABLET in 1 BOTTLE (13668-171-10)
30 TABLET in 1 BOTTLE (13668-171-30)
60 TABLET in 1 BOTTLE (13668-171-60)

source: ndc

Packages (5)

13668-171-01 100 TABLET in 1 BOTTLE (13668-171-01) 13668-171-05 500 TABLET in 1 BOTTLE (13668-171-05) 13668-171-10 1000 TABLET in 1 BOTTLE (13668-171-10) 13668-171-30 30 TABLET in 1 BOTTLE (13668-171-30) 13668-171-60 60 TABLET in 1 BOTTLE (13668-171-60)

Ingredients (1)

olanzapine (20 mg/1)

Linked Drug Pages (1)

OLANZAPINE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "1a64829a-2434-4c8d-8e58-9b28758e4b88", "openfda": {"nui": ["N0000175430"], "upc": ["0313668088304", "0313668170306", "0313668169300", "0313668171303", "0313668168303", "0313668166309", "0313668090307", "0313668089301", "0313668167306", "0313668086300"], "unii": ["N7U69T4SZR"], "rxcui": ["200034", "283639", "312076", "312077", "312078", "312079", "314154", "314155", "351107", "351108"], "spl_set_id": ["2cb1bebe-0ced-46d8-bf21-c28a9acc4a15"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (13668-171-01)", "package_ndc": "13668-171-01", "marketing_start_date": "20260228"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (13668-171-05)", "package_ndc": "13668-171-05", "marketing_start_date": "20260228"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (13668-171-10)", "package_ndc": "13668-171-10", "marketing_start_date": "20260228"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (13668-171-30)", "package_ndc": "13668-171-30", "marketing_start_date": "20260228"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (13668-171-60)", "package_ndc": "13668-171-60", "marketing_start_date": "20260228"}], "brand_name": "OLANZAPINE", "product_id": "13668-171_1a64829a-2434-4c8d-8e58-9b28758e4b88", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "13668-171", "generic_name": "OLANZAPINE", "labeler_name": "Torrent Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OLANZAPINE", "active_ingredients": [{"name": "OLANZAPINE", "strength": "20 mg/1"}], "application_number": "ANDA091434", "marketing_category": "ANDA", "marketing_start_date": "20260228", "listing_expiration_date": "20271231"}