Home NDC 17478-064-12 Gonak Hypromellose
Product NDC 17478-064
Requested package NDC 17478-064-12
11-digit product format 174780064
Labeler code 17478
Product ID 17478-064_7804e6db-6cc3-4d9c-a5fe-df0a8279350c
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Hypromellose 2906 (4000 MPA.S) and Hypromellose 2906 (50 MPA.S)
Dosage form SOLUTION
Route OPHTHALMIC
Labeler Akorn
Marketing category UNAPPROVED DRUG OTHER
Marketing start 1997-01-01
Marketing end 0000-00-00
Substance HYPROMELLOSE 2906 (4000 MPA.S); HYPROMELLOSE 2906 (50 MPA.S)
Active strength 25 mg/mL; mg/mL
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 · 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…
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Hypromellose 2906 (4000 MPA.S) ACTIVE INGREDIENT 5EYA69XGAT GONAK HYPROMELLOSE (HYPROMELLOSE 2906 (4000 MPA.S) AND HYPROMELLOSE 2906 (50 MPA.S)) SOLUTION [AKORN, INC.] 1 Hypromellose 2906 (50 MPA.S) ACTIVE INGREDIENT 612E703ZUQ GONAK HYPROMELLOSE (HYPROMELLOSE 2906 (4000 MPA.S) AND HYPROMELLOSE 2906 (50 MPA.S)) SOLUTION [AKORN, INC.] 1 Hypromellose 2906 (4000 MPA.S) ACTIVE MOIETY 5EYA69XGAT GONAK HYPROMELLOSE (HYPROMELLOSE 2906 (4000 MPA.S) AND HYPROMELLOSE 2906 (50 MPA.S)) SOLUTION [AKORN, INC.] 1 Hypromellose 2906 (50 MPA.S) ACTIVE MOIETY 612E703ZUQ GONAK HYPROMELLOSE (HYPROMELLOSE 2906 (4000 MPA.S) AND HYPROMELLOSE 2906 (50 MPA.S)) SOLUTION [AKORN, INC.] 1 boric acid INACTIVE INGREDIENT R57ZHV85D4 GONAK HYPROMELLOSE (HYPROMELLOSE 2906 (4000 MPA.S) AND HYPROMELLOSE 2906 (50 MPA.S)) SOLUTION [AKORN, INC.] 1 edetate disodium INACTIVE INGREDIENT 7FLD91C86K GONAK HYPROMELLOSE (HYPROMELLOSE 2906 (4000 MPA.S) AND HYPROMELLOSE 2906 (50 MPA.S)) SOLUTION [AKORN, INC.] 1 hydrochloric acid INACTIVE INGREDIENT QTT17582CB GONAK HYPROMELLOSE (HYPROMELLOSE 2906 (4000 MPA.S) AND HYPROMELLOSE 2906 (50 MPA.S)) SOLUTION [AKORN, INC.] 1 potassium chloride INACTIVE INGREDIENT 660YQ98I10 GONAK HYPROMELLOSE (HYPROMELLOSE 2906 (4000 MPA.S) AND HYPROMELLOSE 2906 (50 MPA.S)) SOLUTION [AKORN, INC.] 1 sodium borate INACTIVE INGREDIENT 91MBZ8H3QO GONAK HYPROMELLOSE (HYPROMELLOSE 2906 (4000 MPA.S) AND HYPROMELLOSE 2906 (50 MPA.S)) SOLUTION [AKORN, INC.] 1 sodium hydroxide INACTIVE INGREDIENT 55X04QC32I GONAK HYPROMELLOSE (HYPROMELLOSE 2906 (4000 MPA.S) AND HYPROMELLOSE 2906 (50 MPA.S)) SOLUTION [AKORN, INC.] 1 water INACTIVE INGREDIENT 059QF0KO0R GONAK HYPROMELLOSE (HYPROMELLOSE 2906 (4000 MPA.S) AND HYPROMELLOSE 2906 (50 MPA.S)) SOLUTION [AKORN, INC.] 1
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 17478-064-12 17478006412 1 VIAL in 1 CARTON (17478-064-12) > 15 mL in 1 VIAL 1 vial 1997-01-01 0000-00-00 No No Current