Home NDC 68180-987-09 DROXIDOPA
Product NDC 68180-987
Requested package NDC 68180-987-09
11-digit product format 681800987
Labeler code 68180
Product ID 68180-987_0098094d-a0c0-4b55-9851-68aaf0109233
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name DROXIDOPA
Dosage form CAPSULE
Route ORAL
Labeler Lupin Pharmaceuticals, Inc.
Application ANDA211652
Marketing category ANDA
Marketing start 2021-09-24
Substance DROXIDOPA
Active strength 100 mg/1
Pharmacologic classes Catecholamines [CS], Increased Blood Pressure [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
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 A211652-001 DROXIDOPA DROXIDOPA 100MG CAPSULE / ORAL 2021-02-18 A211652-002 DROXIDOPA DROXIDOPA 200MG CAPSULE / ORAL 2021-02-18 A211652-003 DROXIDOPA DROXIDOPA 300MG CAPSULE / ORAL 2021-02-18
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 3 · 102 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 2026-02-19 14:30 UTC 2026-02 A211652-001 DROXIDOPA 100MG CAPSULE / ORAL 2021-02-18 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A211652-002 DROXIDOPA 200MG CAPSULE / ORAL 2021-02-18 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A211652-003 DROXIDOPA 300MG CAPSULE / ORAL 2021-02-18 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A211652-001 DROXIDOPA 100MG CAPSULE / ORAL AB 2021-02-18 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A211652-002 DROXIDOPA 200MG CAPSULE / ORAL AB 2021-02-18 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A211652-003 DROXIDOPA 300MG CAPSULE / ORAL AB 2021-02-18 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A211652-001 DROXIDOPA 100MG CAPSULE / ORAL AB 2021-02-18 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A211652-002 DROXIDOPA 200MG CAPSULE / ORAL AB 2021-02-18 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A211652-003 DROXIDOPA 300MG CAPSULE / ORAL AB 2021-02-18 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A211652-001 DROXIDOPA 100MG CAPSULE / ORAL AB 2021-02-18 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A211652-002 DROXIDOPA 200MG CAPSULE / ORAL AB 2021-02-18 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A211652-003 DROXIDOPA 300MG CAPSULE / ORAL AB 2021-02-18 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A211652-001 DROXIDOPA 100MG CAPSULE / ORAL AB 2021-02-18 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A211652-002 DROXIDOPA 200MG CAPSULE / ORAL AB 2021-02-18 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A211652-003 DROXIDOPA 300MG CAPSULE / ORAL AB 2021-02-18 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A211652-001 DROXIDOPA 100MG CAPSULE / ORAL AB 2021-02-18 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A211652-002 DROXIDOPA 200MG CAPSULE / ORAL AB 2021-02-18 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A211652-003 DROXIDOPA 300MG CAPSULE / ORAL AB 2021-02-18 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A211652-001 DROXIDOPA 100MG CAPSULE / ORAL AB 2021-02-18 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A211652-002 DROXIDOPA 200MG CAPSULE / ORAL AB 2021-02-18 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A211652-003 DROXIDOPA 300MG CAPSULE / ORAL AB 2021-02-18 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A211652-001 DROXIDOPA 100MG CAPSULE / ORAL AB 2021-02-18 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A211652-002 DROXIDOPA 200MG CAPSULE / ORAL AB 2021-02-18 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A211652-003 DROXIDOPA 300MG CAPSULE / ORAL AB 2021-02-18 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A211652-001 DROXIDOPA 100MG CAPSULE / ORAL AB 2021-02-18 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A211652-002 DROXIDOPA 200MG CAPSULE / ORAL AB 2021-02-18 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A211652-003 DROXIDOPA 300MG CAPSULE / ORAL AB 2021-02-18 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A211652-001 DROXIDOPA 100MG CAPSULE / ORAL AB 2021-02-18 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A211652-002 DROXIDOPA 200MG CAPSULE / ORAL AB 2021-02-18 d06236e962d9…2024-10-29 15:01 UTC 2024-10 A211652-003 DROXIDOPA 300MG CAPSULE / ORAL AB 2021-02-18 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A211652-001 DROXIDOPA 100MG CAPSULE / ORAL AB 2021-02-18 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A211652-002 DROXIDOPA 200MG CAPSULE / ORAL AB 2021-02-18 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A211652-003 DROXIDOPA 300MG CAPSULE / ORAL AB 2021-02-18 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A211652-001 DROXIDOPA 100MG CAPSULE / ORAL AB 2021-02-18 301d65b070ca…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A211652-002 DROXIDOPA 200MG CAPSULE / ORAL AB 2021-02-18 301d65b070ca…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A211652-003 DROXIDOPA 300MG CAPSULE / ORAL AB 2021-02-18 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A211652-001 DROXIDOPA 100MG CAPSULE / ORAL AB 2021-02-18 1e350fbaab3a…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A211652-002 DROXIDOPA 200MG CAPSULE / ORAL AB 2021-02-18 1e350fbaab3a…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A211652-003 DROXIDOPA 300MG CAPSULE / ORAL AB 2021-02-18 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 A211652-001 DROXIDOPA 100MG CAPSULE / ORAL AB 2021-02-18 8072bd15b7f6…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 3 · 96 observed states.
Additional Listing Data#
Finished product Yes
Brand name base DROXIDOPA
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DROXIDOPA 100 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination J7A92W69L7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1490026 Internal RxNorm lookup 1490034 Internal RxNorm lookup 1490038 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 68180-987-02 DROXIDOPA 500 in 1 BOTTLE CAPSULE 500 6 68180-987-09 DROXIDOPA 90 in 1 BOTTLE CAPSULE 90 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68180-987 DROXIDOPA CAPSULE [LUPIN PHARMACEUTICALS, INC.] 6 Current NDC, Legacy NDC, 2 package rows 20231220_81b798dc-b8dc-48a5-af46-82bb55f789a8.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 · 1 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 68180-987-09 68180098709 90 CAPSULE in 1 BOTTLE (68180-987-09) 90 capsule 2021-09-24 0000-00-00 No No Current