Home NDC 68850-012 Myambutol
Product NDC 68850-012
11-digit product format 688500012
Labeler code 68850
Product ID 68850-012_d811b183-f875-3ea9-e053-2995a90af90f
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Ethambutol hydrochloride
Dosage form TABLET, FILM COATED
Route ORAL
Labeler STI Pharma, LLC
Application NDA016320
Marketing category NDA
Marketing start 2007-08-10
Marketing end 0000-00-00
Substance ETHAMBUTOL HYDROCHLORIDE
Active strength 400 mg/1
Pharmacologic classes Antimycobacterial [EPC]
NDC exclude flag No
Listing certified through 2023-12-31
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 · 33 matching rows.
View current auxiliary records. · View the auxiliary file history.
Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 4 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N016320-001 MYAMBUTOL ETHAMBUTOL HYDROCHLORIDE 100MG TABLET / ORAL AB RLD, Approved before 1982 N016320-002 MYAMBUTOL ETHAMBUTOL HYDROCHLORIDE 200MG TABLET / ORAL Approved before 1982 N016320-003 MYAMBUTOL ETHAMBUTOL HYDROCHLORIDE 400MG TABLET / ORAL AB RLD, RS, Approved before 1982 N016320-004 MYAMBUTOL ETHAMBUTOL HYDROCHLORIDE 500MG TABLET / ORAL Approved before 1982
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 1 of 5 · 164 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 N016320-001 MYAMBUTOL 100MG TABLET / ORAL AB RLD, Approved before 1982 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N016320-002 MYAMBUTOL 200MG TABLET / ORAL Approved before 1982 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N016320-003 MYAMBUTOL 400MG TABLET / ORAL AB RLD, RS, Approved before 1982 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N016320-004 MYAMBUTOL 500MG TABLET / ORAL Approved before 1982 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N016320-001 MYAMBUTOL 100MG TABLET / ORAL AB RLD, Approved before 1982 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N016320-002 MYAMBUTOL 200MG TABLET / ORAL Approved before 1982 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N016320-003 MYAMBUTOL 400MG TABLET / ORAL AB RLD, RS, Approved before 1982 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N016320-004 MYAMBUTOL 500MG TABLET / ORAL Approved before 1982 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 N016320-001 MYAMBUTOL 100MG TABLET / ORAL AB RLD, Approved before 1982 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N016320-002 MYAMBUTOL 200MG TABLET / ORAL Approved before 1982 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N016320-003 MYAMBUTOL 400MG TABLET / ORAL AB RLD, RS, Approved before 1982 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N016320-004 MYAMBUTOL 500MG TABLET / ORAL Approved before 1982 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N016320-001 MYAMBUTOL 100MG TABLET / ORAL AB RLD, Approved before 1982 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N016320-002 MYAMBUTOL 200MG TABLET / ORAL Approved before 1982 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N016320-003 MYAMBUTOL 400MG TABLET / ORAL AB RLD, RS, Approved before 1982 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N016320-004 MYAMBUTOL 500MG TABLET / ORAL Approved before 1982 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N016320-001 MYAMBUTOL 100MG TABLET / ORAL AB RLD, Approved before 1982 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N016320-002 MYAMBUTOL 200MG TABLET / ORAL Approved before 1982 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N016320-003 MYAMBUTOL 400MG TABLET / ORAL AB RLD, RS, Approved before 1982 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N016320-004 MYAMBUTOL 500MG TABLET / ORAL Approved before 1982 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N016320-001 MYAMBUTOL 100MG TABLET / ORAL AB RLD, Approved before 1982 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N016320-002 MYAMBUTOL 200MG TABLET / ORAL Approved before 1982 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N016320-003 MYAMBUTOL 400MG TABLET / ORAL AB RLD, RS, Approved before 1982 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N016320-004 MYAMBUTOL 500MG TABLET / ORAL Approved before 1982 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N016320-001 MYAMBUTOL 100MG TABLET / ORAL AB RLD, Approved before 1982 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N016320-002 MYAMBUTOL 200MG TABLET / ORAL Approved before 1982 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N016320-003 MYAMBUTOL 400MG TABLET / ORAL AB RLD, RS, Approved before 1982 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N016320-004 MYAMBUTOL 500MG TABLET / ORAL Approved before 1982 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N016320-001 MYAMBUTOL 100MG TABLET / ORAL AB RLD, Approved before 1982 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N016320-002 MYAMBUTOL 200MG TABLET / ORAL Approved before 1982 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N016320-003 MYAMBUTOL 400MG TABLET / ORAL AB RLD, RS, Approved before 1982 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N016320-004 MYAMBUTOL 500MG TABLET / ORAL Approved before 1982 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N016320-001 MYAMBUTOL 100MG TABLET / ORAL AB RLD, Approved before 1982 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N016320-002 MYAMBUTOL 200MG TABLET / ORAL Approved before 1982 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N016320-003 MYAMBUTOL 400MG TABLET / ORAL AB RLD, RS, Approved before 1982 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N016320-004 MYAMBUTOL 500MG TABLET / ORAL Approved before 1982 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 N016320-001 MYAMBUTOL 100MG TABLET / ORAL AB RLD, Approved before 1982 d06236e962d9…2024-10-29 15:01 UTC 2024-10 N016320-002 MYAMBUTOL 200MG TABLET / ORAL Approved before 1982 d06236e962d9…2024-10-29 15:01 UTC 2024-10 N016320-003 MYAMBUTOL 400MG TABLET / ORAL AB RLD, RS, Approved before 1982 d06236e962d9…2024-10-29 15:01 UTC 2024-10 N016320-004 MYAMBUTOL 500MG TABLET / ORAL Approved before 1982 d06236e962d9…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 3 · 82 observed states.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ETHAMBUTOL HYDROCHLORIDE ACTIVE INGREDIENT QE4VW5FO07 MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET, FILM COATED [STI PHARMA, LLC] 3 ETHAMBUTOL ACTIVE MOIETY 8G167061QZ MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET, FILM COATED [STI PHARMA, LLC] 3 GELATIN INACTIVE INGREDIENT 2G86QN327L MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET, FILM COATED [STI PHARMA, LLC] 3 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET, FILM COATED [STI PHARMA, LLC] 3 SORBITOL INACTIVE INGREDIENT 506T60A25R MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET, FILM COATED [STI PHARMA, LLC] 3 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET, FILM COATED [STI PHARMA, LLC] 3 SUCROSE INACTIVE INGREDIENT C151H8M554 MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET, FILM COATED [STI PHARMA, LLC] 3 ETHAMBUTOL HYDROCHLORIDE ACTIVE INGREDIENT QE4VW5FO07 MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET [PHYSICIANS TOTAL CARE, INC.] 1 ETHAMBUTOL ACTIVE MOIETY 8G167061QZ MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET [PHYSICIANS TOTAL CARE, INC.] 1 GELATIN INACTIVE INGREDIENT 2G86QN327L MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET [PHYSICIANS TOTAL CARE, INC.] 1 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET [PHYSICIANS TOTAL CARE, INC.] 1 MAGNESIUM STEARATE INACTIVE INGREDIENT 70097M6I30 MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET [PHYSICIANS TOTAL CARE, INC.] 1 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET [PHYSICIANS TOTAL CARE, INC.] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET [PHYSICIANS TOTAL CARE, INC.] 1 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET [PHYSICIANS TOTAL CARE, INC.] 1 SUCROSE INACTIVE INGREDIENT C151H8M554 MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET [PHYSICIANS TOTAL CARE, INC.] 1 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP MYAMBUTOL (ETHAMBUTOL HYDROCHLORIDE) TABLET [PHYSICIANS TOTAL CARE, INC.] 1
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 · 3 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 68850-012-01 68850001201 100 TABLET, FILM COATED in 1 BOTTLE (68850-012-01) 2007-08-10 0000-00-00 No No Current 68850-012-02 68850001202 10 BLISTER PACK in 1 BOX, UNIT-DOSE (68850-012-02) > 10 TABLET, FILM COATED in 1 BLISTER PACK 10 blister pack 2007-08-10 0000-00-00 No No Current