entecavir
Generic: entecavir
Labeler: cipla usa inc.Drug Facts
Product Profile
Brand Name
entecavir
Generic Name
entecavir
Labeler
cipla usa inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
entecavir .5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69097-426
Product ID
69097-426_f11e1153-612f-4924-86b1-6739d755e3c1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206872
Listing Expiration
2026-12-31
Marketing Start
2016-12-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69097426
Hyphenated Format
69097-426
Supplemental Identifiers
RxCUI
UPC
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
entecavir (source: ndc)
Generic Name
entecavir (source: ndc)
Application Number
ANDA206872 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69097-426-02)
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69097-426-05)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f11e1153-612f-4924-86b1-6739d755e3c1", "openfda": {"upc": ["0369097425029", "0369097426026", "0369097426057"], "unii": ["5968Y6H45M"], "rxcui": ["485434", "485436"], "spl_set_id": ["d59e9ea4-09ea-47bd-af2f-39f7a2e2aceb"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69097-426-02)", "package_ndc": "69097-426-02", "marketing_start_date": "20161206"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69097-426-05)", "package_ndc": "69097-426-05", "marketing_start_date": "20161206"}], "brand_name": "ENTECAVIR", "product_id": "69097-426_f11e1153-612f-4924-86b1-6739d755e3c1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]", "Nucleoside Analog [EXT]", "Nucleoside Reverse Transcriptase Inhibitors [MoA]"], "product_ndc": "69097-426", "generic_name": "ENTECAVIR", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ENTECAVIR", "active_ingredients": [{"name": "ENTECAVIR", "strength": ".5 mg/1"}], "application_number": "ANDA206872", "marketing_category": "ANDA", "marketing_start_date": "20161206", "listing_expiration_date": "20261231"}