Home NDC 66343-002 Geovita
Product NDC 66343-002
11-digit product format 663430002
Labeler code 66343
Product ID 66343-002_6ec595e1-0851-4637-b51e-3971b760af1c
Type HUMAN OTC DRUG
Nonproprietary name IRON, SILICON DIOXIDE, COPPER, FORMIC ACID, and SUS SCROFA CEREBELLUM
Dosage form LIQUID
Route ORAL
Labeler RUBIMED AG
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-05-07
Marketing end 0000-00-00
Substance IRON; SILICON DIOXIDE; COPPER; FORMIC ACID; SUS SCROFA CEREBELLUM
Active strength 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag E
Listing certified through 2017-12-31
Current FDA listing Historical FDA.report record 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 · 44 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 66343-002-50 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 66343-002-50 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 66343-002-50 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 66343-002-50 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 66343-002-50 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 66343-002-50 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product D Discontinued by firm 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 66343-002-50 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 66343-002-50 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 66343-002-50 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 66343-002-50 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 66343-002-50 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 66343-002-50 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 66343-002-50 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product I Inactivated by FDA 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 66343-002-50 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 66343-002-50 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 66343-002-50 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 66343-002-50 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 66343-002-50 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 66343-002-50 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 66343-002-50 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 66343-002-50 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 66343-002-50 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded COPPER ACTIVE INGREDIENT 789U1901C5 GEOVITA (IRON, SILICON DIOXIDE, COPPER, FORMIC ACID, AND SUS SCROFA CEREBELLUM) LIQUID [RUBIMED AG] 1 FORMIC ACID ACTIVE INGREDIENT 0YIW783RG1 GEOVITA (IRON, SILICON DIOXIDE, COPPER, FORMIC ACID, AND SUS SCROFA CEREBELLUM) LIQUID [RUBIMED AG] 1 IRON ACTIVE INGREDIENT E1UOL152H7 GEOVITA (IRON, SILICON DIOXIDE, COPPER, FORMIC ACID, AND SUS SCROFA CEREBELLUM) LIQUID [RUBIMED AG] 1 SILICON DIOXIDE ACTIVE INGREDIENT ETJ7Z6XBU4 GEOVITA (IRON, SILICON DIOXIDE, COPPER, FORMIC ACID, AND SUS SCROFA CEREBELLUM) LIQUID [RUBIMED AG] 1 SUS SCROFA CEREBELLUM ACTIVE INGREDIENT 49NGK53TPQ GEOVITA (IRON, SILICON DIOXIDE, COPPER, FORMIC ACID, AND SUS SCROFA CEREBELLUM) LIQUID [RUBIMED AG] 1 COPPER ACTIVE MOIETY 789U1901C5 GEOVITA (IRON, SILICON DIOXIDE, COPPER, FORMIC ACID, AND SUS SCROFA CEREBELLUM) LIQUID [RUBIMED AG] 1 FORMIC ACID ACTIVE MOIETY 0YIW783RG1 GEOVITA (IRON, SILICON DIOXIDE, COPPER, FORMIC ACID, AND SUS SCROFA CEREBELLUM) LIQUID [RUBIMED AG] 1 IRON ACTIVE MOIETY E1UOL152H7 GEOVITA (IRON, SILICON DIOXIDE, COPPER, FORMIC ACID, AND SUS SCROFA CEREBELLUM) LIQUID [RUBIMED AG] 1 SILICON DIOXIDE ACTIVE MOIETY ETJ7Z6XBU4 GEOVITA (IRON, SILICON DIOXIDE, COPPER, FORMIC ACID, AND SUS SCROFA CEREBELLUM) LIQUID [RUBIMED AG] 1 SUS SCROFA CEREBELLUM ACTIVE MOIETY 49NGK53TPQ GEOVITA (IRON, SILICON DIOXIDE, COPPER, FORMIC ACID, AND SUS SCROFA CEREBELLUM) LIQUID [RUBIMED AG] 1 ALCOHOL INACTIVE INGREDIENT 3K9958V90M GEOVITA (IRON, SILICON DIOXIDE, COPPER, FORMIC ACID, AND SUS SCROFA CEREBELLUM) LIQUID [RUBIMED AG] 1