ZERIT

Product NDC: 0003-1966
11-digit product format: 000031966
Labeler code: 0003
Product ID: 0003-1966_41d3b607-aa70-408b-9e05-c3e285482568
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: stavudine
Dosage form: CAPSULE, GELATIN COATED
Route: ORAL
Labeler: E.R. Squibb & Sons, L.L.C.
Application: NDA020412
Marketing category: NDA
Marketing start: 1994-06-24
Marketing end: 2020-09-30
Substance: STAVUDINE
Active strength: 30 mg/1
Pharmacologic classes: Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]
NDC exclude flag: No
Listing certified through: 0000-00-00
Current FDA listing: Historical FDA.report record

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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	0003-1966		D	Discontinued by firm		2026-10-05
excluded package	package	0003-1966	0003-1966-01	D	Discontinued by firm		2026-10-05

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 · 24 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	0003-1966-01	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	0003-1966-01	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	0003-1966-01	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	0003-1966-01	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	0003-1966-01	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	0003-1966-01	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	0003-1966-01	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	0003-1966-01	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	0003-1966-01	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	0003-1966-01	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	0003-1966-01	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	0003-1966-01	`557ba5c1ecfa…`	`9c80585c8c6e…`

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 5 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	RLD / RS	Approval date
N020412-001	ZERIT	STAVUDINE	5MG	CAPSULE / ORAL		1994-06-24
N020412-002	ZERIT	STAVUDINE	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24
N020412-003	ZERIT	STAVUDINE	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24
N020412-004	ZERIT	STAVUDINE	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24
N020412-005	ZERIT	STAVUDINE	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24

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 6 · 215 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	RLD / RS	Approval date	Source SHA-256
2026-09-14 22:38:34	2026-08	N020412-001	ZERIT	5MG	CAPSULE / ORAL		1994-06-24	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N020412-002	ZERIT	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N020412-003	ZERIT	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N020412-004	ZERIT	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N020412-005	ZERIT	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	N020412-001	ZERIT	5MG	CAPSULE / ORAL		1994-06-24	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N020412-002	ZERIT	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N020412-003	ZERIT	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N020412-004	ZERIT	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N020412-005	ZERIT	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	N020412-001	ZERIT	5MG	CAPSULE / ORAL		1994-06-24	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020412-002	ZERIT	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020412-003	ZERIT	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020412-004	ZERIT	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020412-005	ZERIT	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020412-001	ZERIT	5MG	CAPSULE / ORAL		1994-06-24	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020412-002	ZERIT	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020412-003	ZERIT	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020412-004	ZERIT	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020412-005	ZERIT	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	N020412-001	ZERIT	5MG	CAPSULE / ORAL		1994-06-24	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020412-002	ZERIT	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020412-003	ZERIT	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020412-004	ZERIT	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020412-005	ZERIT	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020412-001	ZERIT	5MG	CAPSULE / ORAL		1994-06-24	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020412-002	ZERIT	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020412-003	ZERIT	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020412-004	ZERIT	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020412-005	ZERIT	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020412-001	ZERIT	5MG	CAPSULE / ORAL		1994-06-24	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020412-002	ZERIT	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020412-003	ZERIT	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020412-004	ZERIT	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020412-005	ZERIT	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020412-001	ZERIT	5MG	CAPSULE / ORAL		1994-06-24	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020412-002	ZERIT	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020412-003	ZERIT	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020412-004	ZERIT	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020412-005	ZERIT	40MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	RLD	1994-06-24	`03ed91905a0d…`

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2019-12-13 00:20 UTC	2019-12	N020412-002	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N020412-003	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N020412-004	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N020412-005	AB	1	`74a2ff9319b5…`
2019-12-14 00:12 UTC	2019-12	N020412-002	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N020412-003	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N020412-004	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N020412-005	AB	1	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	N020412-002	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N020412-003	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N020412-004	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N020412-005	AB	1	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	N020412-002	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N020412-003	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N020412-004	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N020412-005	AB	1	`ea99ee380514…`

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
4f7bbe6f-8bb8-eee9-cb0e-a5f4e0b695d8	Product name	1	20140508

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0003-1966-01	EA - Each	0003-1966	a0788ddc-3885-480c-b28f-4cfea81248ab	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
stavudine	ACTIVE INGREDIENT	BO9LE4QFZF	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) POWDER, FOR SOLUTION [E.R. SQUIBB & SONS, L.L.C.]	23
stavudine	ACTIVE MOIETY	BO9LE4QFZF	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) POWDER, FOR SOLUTION [E.R. SQUIBB & SONS, L.L.C.]	23
carboxymethylcellulose sodium	INACTIVE INGREDIENT	K679OBS311	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) POWDER, FOR SOLUTION [E.R. SQUIBB & SONS, L.L.C.]	23
cellulose, microcrystalline	INACTIVE INGREDIENT	OP1R32D61U	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) POWDER, FOR SOLUTION [E.R. SQUIBB & SONS, L.L.C.]	23
gelatin	INACTIVE INGREDIENT	2G86QN327L	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) POWDER, FOR SOLUTION [E.R. SQUIBB & SONS, L.L.C.]	23
lactose	INACTIVE INGREDIENT	J2B2A4N98G	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) POWDER, FOR SOLUTION [E.R. SQUIBB & SONS, L.L.C.]	23
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) POWDER, FOR SOLUTION [E.R. SQUIBB & SONS, L.L.C.]	23
methylparaben	INACTIVE INGREDIENT	A2I8C7HI9T	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) POWDER, FOR SOLUTION [E.R. SQUIBB & SONS, L.L.C.]	23
propylparaben	INACTIVE INGREDIENT	Z8IX2SC1OH	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) POWDER, FOR SOLUTION [E.R. SQUIBB & SONS, L.L.C.]	23
sodium starch glycolate type A potato	INACTIVE INGREDIENT	5856J3G2A2	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) POWDER, FOR SOLUTION [E.R. SQUIBB & SONS, L.L.C.]	23
sucrose	INACTIVE INGREDIENT	C151H8M554	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) POWDER, FOR SOLUTION [E.R. SQUIBB & SONS, L.L.C.]	23
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) CAPSULE, GELATIN COATED ZERIT (STAVUDINE) POWDER, FOR SOLUTION [E.R. SQUIBB & SONS, L.L.C.]	23
STAVUDINE	ACTIVE INGREDIENT	BO9LE4QFZF	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	3
stavudine	ACTIVE MOIETY	BO9LE4QFZF	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	3
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	3
GELATIN	INACTIVE INGREDIENT	2G86QN327L	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	3
LACTOSE	INACTIVE INGREDIENT	J2B2A4N98G	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	3
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	3
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	3
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	ZERIT (STAVUDINE) CAPSULE, GELATIN COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY]	3

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
BO9LE4QFZF	STAVUDINE	3056-17-5	STAVUDINE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
313108	stavudine 20 MG Oral Capsule	PSN	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
313109	stavudine 30 MG Oral Capsule	PSN	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
313110	stavudine 40 MG Oral Capsule	PSN	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
152942	Zerit 20 MG Oral Capsule	PSN	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
152943	Zerit 30 MG Oral Capsule	PSN	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
152944	Zerit 40 MG Oral Capsule	PSN	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
152942	stavudine 20 MG Oral Capsule [Zerit]	SBD	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
152943	stavudine 30 MG Oral Capsule [Zerit]	SBD	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
152944	stavudine 40 MG Oral Capsule [Zerit]	SBD	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
313108	stavudine 20 MG Oral Capsule	SCD	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
313109	stavudine 30 MG Oral Capsule	SCD	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
313110	stavudine 40 MG Oral Capsule	SCD	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
313108	D4T 20 MG Oral Capsule	SY	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
152942	D4T 20 MG Oral Capsule [Zerit]	SY	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
313109	D4T 30 MG Oral Capsule	SY	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
152943	D4T 30 MG Oral Capsule [Zerit]	SY	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
313110	D4T 40 MG Oral Capsule	SY	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
152944	D4T 40 MG Oral Capsule [Zerit]	SY	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
313108	DHT 20 MG Oral Capsule	SY	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
152942	DHT 20 MG Oral Capsule [Zerit]	SY	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
313109	DHT 30 MG Oral Capsule	SY	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
152943	DHT 30 MG Oral Capsule [Zerit]	SY	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
313110	DHT 40 MG Oral Capsule	SY	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
152944	DHT 40 MG Oral Capsule [Zerit]	SY	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
152942	Zerit 20 MG Oral Capsule	SY	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
152943	Zerit 30 MG Oral Capsule	SY	8bb73c56-74cb-4602-b9a3-57bd1082b434	3
152944	Zerit 40 MG Oral Capsule	SY	8bb73c56-74cb-4602-b9a3-57bd1082b434	3

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
ZERIT	E.R. Squibb & Sons, L.L.C.	2018-12-17	HUMAN PRESCRIPTION DRUG LABEL	29
ZERIT ® (stavudine) Capsules ZERIT ® (stavudine) for Oral Solution	State of Florida DOH Central Pharmacy	2010-08-12	HUMAN PRESCRIPTION DRUG LABEL	3