lamivudine

Generic: lamivudine

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lamivudine
Generic Name lamivudine
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

lamivudine 100 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-001
Product ID 31722-001_2b449c4a-56db-0d5f-e063-6394a90ad576
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211306
Listing Expiration 2026-12-31
Marketing Start 2019-03-21

Pharmacologic Class

Established (EPC)
hepatitis b virus nucleoside analog reverse transcriptase inhibitor [epc] human immunodeficiency virus nucleoside analog reverse transcriptase inhibitor [epc]
Mechanism of Action
nucleoside reverse transcriptase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722001
Hyphenated Format 31722-001

Supplemental Identifiers

RxCUI
205328
UPC
0331722001601
UNII
2T8Q726O95
NUI
N0000175656 N0000175462 N0000009947

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 lamivudine (source: ndc)
Generic Name lamivudine (source: ndc)
Application Number ANDA211306 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 20 BLISTER PACK in 1 CARTON (31722-001-02) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • 60 TABLET, FILM COATED in 1 BOTTLE (31722-001-60)
source: ndc

Packages (2)

31722-001-02 20 BLISTER PACK in 1 CARTON (31722-001-02) / 10 TABLET, FILM COATED in 1 BLISTER PACK 31722-001-60 60 TABLET, FILM COATED in 1 BOTTLE (31722-001-60)

Ingredients (1)

lamivudine (100 mg/1)

Linked Drug Pages (1)

lamivudine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2b449c4a-56db-0d5f-e063-6394a90ad576", "openfda": {"nui": ["N0000175656", "N0000175462", "N0000009947"], "upc": ["0331722001601"], "unii": ["2T8Q726O95"], "rxcui": ["205328"], "spl_set_id": ["e90671c6-7fff-48f4-8898-29f02d049c8b"], "pharm_class_epc": ["Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]", "Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]"], "pharm_class_moa": ["Nucleoside Reverse Transcriptase Inhibitors [MoA]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 CARTON (31722-001-02)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "31722-001-02", "marketing_start_date": "20190321"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (31722-001-60)", "package_ndc": "31722-001-60", "marketing_start_date": "20190321"}], "brand_name": "lamivudine", "product_id": "31722-001_2b449c4a-56db-0d5f-e063-6394a90ad576", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]", "Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC]", "Nucleoside Reverse Transcriptase Inhibitors [MoA]"], "product_ndc": "31722-001", "generic_name": "lamivudine", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "lamivudine", "active_ingredients": [{"name": "LAMIVUDINE", "strength": "100 mg/1"}], "application_number": "ANDA211306", "marketing_category": "ANDA", "marketing_start_date": "20190321", "listing_expiration_date": "20261231"}