Home NDC 59762-2135 amlodipine besylate
Product NDC 59762-2135
11-digit product format 597622135
Labeler code 59762
Product ID 59762-2135_4826ff96-be7a-460d-8ec0-d6bd025d1162
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name amlodipine besylate
Dosage form TABLET
Route ORAL
Labeler Mylan Pharmaceuticals Inc.
Application NDA019787
Marketing category NDA AUTHORIZED GENERIC
Marketing start 2019-06-24
Substance AMLODIPINE BESYLATE
Active strength 10 mg/1
Pharmacologic classes Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 42 .
Orange Book products# Current product rows page 1 of 1 · 3 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N019787-001 NORVASC AMLODIPINE BESYLATE EQ 2.5MG BASE TABLET / ORAL AB RLD 1992-07-31 N019787-002 NORVASC AMLODIPINE BESYLATE EQ 5MG BASE TABLET / ORAL AB RLD 1992-07-31 N019787-003 NORVASC AMLODIPINE BESYLATE EQ 10MG BASE TABLET / ORAL AB RLD, RS 1992-07-31
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 3 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 1 of 4 · 126 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 2026-08-18 06:07:40 2026-07 N019787-001 NORVASC EQ 2.5MG BASE TABLET / ORAL AB RLD 1992-07-31 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N019787-002 NORVASC EQ 5MG BASE TABLET / ORAL AB RLD 1992-07-31 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N019787-003 NORVASC EQ 10MG BASE TABLET / ORAL AB RLD, RS 1992-07-31 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 N019787-001 NORVASC EQ 2.5MG BASE TABLET / ORAL AB RLD 1992-07-31 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N019787-002 NORVASC EQ 5MG BASE TABLET / ORAL AB RLD 1992-07-31 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N019787-003 NORVASC EQ 10MG BASE TABLET / ORAL AB RLD, RS 1992-07-31 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N019787-001 NORVASC EQ 2.5MG BASE TABLET / ORAL AB RLD 1992-07-31 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N019787-002 NORVASC EQ 5MG BASE TABLET / ORAL AB RLD 1992-07-31 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N019787-003 NORVASC EQ 10MG BASE TABLET / ORAL AB RLD, RS 1992-07-31 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 N019787-001 NORVASC EQ 2.5MG BASE TABLET / ORAL AB RLD 1992-07-31 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N019787-002 NORVASC EQ 5MG BASE TABLET / ORAL AB RLD 1992-07-31 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N019787-003 NORVASC EQ 10MG BASE TABLET / ORAL AB RLD, RS 1992-07-31 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N019787-001 NORVASC EQ 2.5MG BASE TABLET / ORAL AB RLD 1992-07-31 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N019787-002 NORVASC EQ 5MG BASE TABLET / ORAL AB RLD 1992-07-31 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N019787-003 NORVASC EQ 10MG BASE TABLET / ORAL AB RLD, RS 1992-07-31 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N019787-001 NORVASC EQ 2.5MG BASE TABLET / ORAL AB RLD 1992-07-31 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N019787-002 NORVASC EQ 5MG BASE TABLET / ORAL AB RLD 1992-07-31 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N019787-003 NORVASC EQ 10MG BASE TABLET / ORAL AB RLD, RS 1992-07-31 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N019787-001 NORVASC EQ 2.5MG BASE TABLET / ORAL AB RLD 1992-07-31 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N019787-002 NORVASC EQ 5MG BASE TABLET / ORAL AB RLD 1992-07-31 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N019787-003 NORVASC EQ 10MG BASE TABLET / ORAL AB RLD, RS 1992-07-31 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N019787-001 NORVASC EQ 2.5MG BASE TABLET / ORAL AB RLD 1992-07-31 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N019787-002 NORVASC EQ 5MG BASE TABLET / ORAL AB RLD 1992-07-31 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N019787-003 NORVASC EQ 10MG BASE TABLET / ORAL AB RLD, RS 1992-07-31 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N019787-001 NORVASC EQ 2.5MG BASE TABLET / ORAL AB RLD 1992-07-31 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N019787-002 NORVASC EQ 5MG BASE TABLET / ORAL AB RLD 1992-07-31 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N019787-003 NORVASC EQ 10MG BASE TABLET / ORAL AB RLD, RS 1992-07-31 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N019787-001 NORVASC EQ 2.5MG BASE TABLET / ORAL AB RLD 1992-07-31 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N019787-002 NORVASC EQ 5MG BASE TABLET / ORAL AB RLD 1992-07-31 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N019787-003 NORVASC EQ 10MG BASE TABLET / ORAL AB RLD, RS 1992-07-31 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 N019787-001 NORVASC EQ 2.5MG BASE TABLET / ORAL AB RLD 1992-07-31 d06236e962d9…2024-10-29 15:01 UTC 2024-10 N019787-002 NORVASC EQ 5MG BASE TABLET / ORAL AB RLD 1992-07-31 d06236e962d9…2024-10-29 15:01 UTC 2024-10 N019787-003 NORVASC EQ 10MG BASE TABLET / ORAL AB RLD, RS 1992-07-31 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N019787-001 NORVASC EQ 2.5MG BASE TABLET / ORAL AB RLD 1992-07-31 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N019787-002 NORVASC EQ 5MG BASE TABLET / ORAL AB RLD 1992-07-31 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N019787-003 NORVASC EQ 10MG BASE TABLET / ORAL AB RLD, RS 1992-07-31 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 N019787-001 NORVASC EQ 2.5MG BASE TABLET / ORAL AB RLD 1992-07-31 301d65b070ca…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 N019787-002 NORVASC EQ 5MG BASE TABLET / ORAL AB RLD 1992-07-31 301d65b070ca…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 N019787-003 NORVASC EQ 10MG BASE TABLET / ORAL AB RLD, RS 1992-07-31 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 N019787-001 NORVASC EQ 2.5MG BASE TABLET / ORAL AB RLD 1992-07-31 1e350fbaab3a…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 4 · 126 observed states.
Additional Listing Data#
Finished product Yes
Brand name base amlodipine besylate
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AMLODIPINE BESYLATE 10 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 864V2Q084H Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 197361 Internal RxNorm lookup 308135 Internal RxNorm lookup 308136 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59762-2135-1 amlodipine besylate 1000 in 1 BOTTLE TABLET 1000 32 59762-2135-9 amlodipine besylate 90 in 1 BOTTLE TABLET 90 32
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59762-2135 AMLODIPINE BESYLATE TABLET [MYLAN PHARMACEUTICALS INC.] 31 Current NDC, Legacy NDC, 2 package rows 20250502_180ee374-24f2-4b9c-9d54-8815f2b1dc9b.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 4 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 59762-2135-1 59762213501 1000 TABLET in 1 BOTTLE (59762-2135-1) 1000 tablet 2019-11-13 0000-00-00 No No Current 59762-2135-9 59762213509 90 TABLET in 1 BOTTLE (59762-2135-9) 90 tablet 2019-06-24 0000-00-00 No No Current