olanzapine
Generic: olanzapine
Labeler: dr. reddy's laboratories inc.Drug Facts
Product Profile
Brand Name
olanzapine
Generic Name
olanzapine
Labeler
dr. reddy's laboratories inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
olanzapine 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43598-166
Product ID
43598-166_9f9b5830-1420-24fc-73be-4a040ccb22db
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076255
Listing Expiration
2026-12-31
Marketing Start
2013-12-10
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43598166
Hyphenated Format
43598-166
Supplemental Identifiers
RxCUI
UNII
NUI
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
olanzapine (source: ndc)
Generic Name
olanzapine (source: ndc)
Application Number
ANDA076255 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE (43598-166-01)
- 500 TABLET, FILM COATED in 1 BOTTLE (43598-166-05)
- 1000 TABLET, FILM COATED in 1 BOTTLE (43598-166-10)
- 30 TABLET, FILM COATED in 1 BOTTLE (43598-166-30)
- 60 TABLET, FILM COATED in 1 BOTTLE (43598-166-60)
- 10 BLISTER PACK in 1 CARTON (43598-166-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-166-79)
Packages (6)
43598-166-01
100 TABLET, FILM COATED in 1 BOTTLE (43598-166-01)
43598-166-05
500 TABLET, FILM COATED in 1 BOTTLE (43598-166-05)
43598-166-10
1000 TABLET, FILM COATED in 1 BOTTLE (43598-166-10)
43598-166-30
30 TABLET, FILM COATED in 1 BOTTLE (43598-166-30)
43598-166-60
60 TABLET, FILM COATED in 1 BOTTLE (43598-166-60)
43598-166-78
10 BLISTER PACK in 1 CARTON (43598-166-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-166-79)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9f9b5830-1420-24fc-73be-4a040ccb22db", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["312078", "312079", "314154"], "spl_set_id": ["d474d5a9-d338-511d-5823-567c0a1bbf4d"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (43598-166-01)", "package_ndc": "43598-166-01", "marketing_start_date": "20131210"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (43598-166-05)", "package_ndc": "43598-166-05", "marketing_start_date": "20131210"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (43598-166-10)", "package_ndc": "43598-166-10", "marketing_start_date": "20131210"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (43598-166-30)", "package_ndc": "43598-166-30", "marketing_start_date": "20131210"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (43598-166-60)", "package_ndc": "43598-166-60", "marketing_start_date": "20131210"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (43598-166-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (43598-166-79)", "package_ndc": "43598-166-78", "marketing_start_date": "20131210"}], "brand_name": "Olanzapine", "product_id": "43598-166_9f9b5830-1420-24fc-73be-4a040ccb22db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "43598-166", "generic_name": "Olanzapine", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "10 mg/1"}], "application_number": "ANDA076255", "marketing_category": "ANDA", "marketing_start_date": "20131210", "listing_expiration_date": "20261231"}