38779-2689-9

Product NDC: 38779-2689
Requested package NDC: 38779-2689-9
11-digit product format: 387792689
Labeler code: 38779
Product ID: 38779-2689_3a9e12ab-a6e7-960b-e063-6294a90afe8f
Type: BULK INGREDIENT
Nonproprietary name: Fenbendazole
Dosage form: POWDER
Marketing category: BULK INGREDIENT
Marketing start: 2014-05-23
Substance: FENBENDAZOLE
Active strength: 1 g/g
Listing certified through: 2026-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
unfinished package	package	38779-2689	38779-2689-9	UNFINISHED	Active or certified unfinished drug listing		2026-10-12

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 · 15 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 21:27 UTC · source 2025-12-05	`a6255e0c9aa5…`	`a0211a219f2e…`
2025-08-26 23:59 UTC · source 2025-08-26	`1d862106b807…`	`00c93037cd84…`
2025-05-15 14:59 UTC · source 2025-05-14	`390b4c401c3f…`	`2c692c2daee3…`
2025-04-01 07:37 UTC · source 2025-03-31	`e30019b0c005…`	`a3f0b14938b7…`
2025-03-01 13:19 UTC · source 2025-02-28	`bbbc9f937eca…`	`946b9c97cf81…`
2025-02-27 05:24 UTC · source 2025-02-26	`f268b84574a6…`	`26285f5ac5df…`
2025-02-01 13:13 UTC · source 2025-01-31	`f764e8902f78…`	`92046438deef…`
2025-01-20 13:05 UTC · source 2025-01-17	`68b1e3bced9e…`	`98a755eb8bc6…`
2024-11-29 20:42 UTC · source 2024-11-29	`05c55d027831…`	`ca05dca9dc4c…`
2024-11-09 02:36 UTC · source 2024-11-08	`48b4f40e6753…`	`c7c7a00d2afa…`
2024-10-09 02:27 UTC · source 2024-10-08	`27f29a85d7e4…`	`1372111e901f…`
2024-07-10 04:00 UTC · source 2024-07-09	`8d62ce987f31…`	`9fe9ef23e30d…`
2024-05-28 21:11 UTC · source 2024-05-28	`d1e113ab4d42…`	`063ee3eb0a1d…`
2024-05-15 03:51 UTC · source 2024-05-14	`50b4072663b7…`	`eae3003ed65e…`
2019-06-01 22:24 UTC · source 2019-05-30	`5b2001dcd8f5…`	`54b53d4dc9e4…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: No
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
FENBENDAZOLE	1 g/g

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
38779-2689-3	GM - Gram	38779-2689	dc6b26cc-d9e4-4023-b498-250352d5de2d	1	2014-06-03
38779-2689-5	GM - Gram	38779-2689	1dfea77c-3553-4b18-8532-bd0c00137c6f	1	2014-06-03
38779-2689-7	GM - Gram	38779-2689	3b25fb83-af8f-44f9-84e5-83ec4bc5b38b	1	2014-09-03
38779-2689-8	GM - Gram	38779-2689	d3543cc3-db9d-4619-b193-9fc0597a2f4d	1	2014-06-03
38779-2689-9	GM - Gram	38779-2689	e9a4935d-cbbd-4fd1-b5d3-1946c4cc4054	1	2014-06-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
FENBENDAZOLE	ACTIVE INGREDIENT	621BVT9M36	FENBENDAZOLE POWDER [MEDISCA INC.]	1
FENBENDAZOLE	ACTIVE MOIETY	621BVT9M36	FENBENDAZOLE POWDER [MEDISCA INC.]	1

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
621BVT9M36	FENBENDAZOLE	43210-67-9	FENBENDAZOLE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Status
38779-2689-9	38779268909	1000 g in 1 JAR (38779-2689-9)	1000 g	09-SEP-16	Current