Home NDC 69097-167 LAMIVUDINE
Product NDC 69097-167
11-digit product format 690970167
Labeler code 69097
Product ID 69097-167_65d03051-a84c-49d7-928b-515cb1769bec
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name LAMIVUDINE
Dosage form TABLET
Route ORAL
Labeler Cipla USA Inc.
Application ANDA077221
Marketing category ANDA
Marketing start 2017-03-03
Marketing end 0000-00-00
Substance LAMIVUDINE
Active strength 300 mg/1
Pharmacologic classes Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]
NDC exclude flag No
Listing certified through 2020-12-31
Current FDA listing Historical FDA.report record
Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
Orange Book products# Current product rows page 1 of 1 · 2 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A077221-001 LAMIVUDINE LAMIVUDINE 150MG TABLET / ORAL AB 2017-03-03 A077221-002 LAMIVUDINE LAMIVUDINE 300MG TABLET / ORAL AB 2017-03-03
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 2 matching rows.
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Product history page 3 of 3 · 86 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2022-09-29 23:25 UTC 2022-09 A077221-001 LAMIVUDINE 150MG TABLET / ORAL AB 2017-03-03 e64feba35796…2022-09-29 23:25 UTC 2022-09 A077221-002 LAMIVUDINE 300MG TABLET / ORAL AB 2017-03-03 e64feba35796…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 A077221-001 LAMIVUDINE 150MG TABLET / ORAL AB 2017-03-03 cb3db0bc1861…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 A077221-002 LAMIVUDINE 300MG TABLET / ORAL AB 2017-03-03 cb3db0bc1861…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A077221-001 LAMIVUDINE 150MG TABLET / ORAL AB 2017-03-03 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A077221-002 LAMIVUDINE 300MG TABLET / ORAL AB 2017-03-03 a50c72e98297…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 3 · 86 observed states.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69097-167 LAMIVUDINE TABLET [CIPLA USA INC.] 9 Legacy NDC 20190610_36b83d9a-962f-4821-bf44-0bace705b620.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69097-167-02 69097016702 30 TABLET in 1 BOTTLE (69097-167-02) 30 tablet 2017-03-03 0000-00-00 No No Current