Tri-Previfem

Product NDC: 53002-2304
11-digit product format: 530022304
Labeler code: 53002
Product ID: 53002-2304_9ed4795c-52cc-41eb-81b8-0f7a928c4aa1
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: norgestimate and ethinyl estradiol
Dosage form: KIT
Labeler: RPK Pharmaceuticals, Inc.
Application: ANDA090793
Marketing category: ANDA
Marketing start: 2019-02-01
Marketing end: 0000-00-00
Active strength: 0
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 4 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	53002-2304		D	Discontinued by firm	2026-07-31
excluded package	package	53002-2304	53002-2304-1	D	Discontinued by firm	2026-07-31
excluded package	package	53002-2304	53002-2304-3	D	Discontinued by firm	2026-07-31
excluded package	package	53002-2304	53002-2304-6	D	Discontinued by firm	2026-07-31

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

Orange Book products#

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

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	RLD / RS	Approval date
A090793-001	TRI-ESTARYLLA	ETHINYL ESTRADIOL; NORGESTIMATE	0.035MG,0.035MG,0.035MG;0.18MG,0.215MG,0.25MG	TABLET / ORAL-28	AB		2013-01-30

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 1 matching rows.

Application-product, TE code table
Application-product	TE code
A090793-001	AB

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.

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
2026-08-01 22:54:32	2026-06	A090793-001	TRI-ESTARYLLA	0.035MG,0.035MG,0.035MG;0.18MG,0.215MG,0.25MG	TABLET / ORAL-28	AB		2013-01-30	`a50c72e98297…`

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2026-08-01 22:54:32	2026-06	A090793-001	AB	1	`a50c72e98297…`

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 4 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Tri-Estarylla	NORGESTIMATE AND ETHINYL ESTRADIOL	A-S Medication Solutions	f7f7c073-48e0-4065-970b-8103d76b6eb0	2026-01-27	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 090793 application number: ANDA090793
Tri-Estarylla	NORGESTIMATE AND ETHINYL ESTRADIOL	Bryant Ranch Prepack	6560d15f-6ce9-4f0e-9b59-043dec35ddd9	2024-05-21	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 090793 application number: ANDA090793
norgestimate and ethinyl estradiol	NORGESTIMATE AND ETHINYL ESTRADIOL	AvKARE	a3cfd79e-a344-1dfc-e053-2995a90a1ab7	2024-01-10	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 090793 application number: ANDA090793
Tri-Estarylla	NORGESTIMATE AND ETHINYL ESTRADIOL	Xiromed, LLC.	1ba8a8ab-eb09-0807-47d4-6b4055d10d91	2023-08-01	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 090793 application number: ANDA090793

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
53002-2304-1	53002230401	1 KIT in 1 BLISTER PACK (53002-2304-1)	1 kit	2019-02-01	0000-00-00	No	No	Current
53002-2304-3	53002230403	3 BLISTER PACK in 1 POUCH (53002-2304-3) > 1 KIT in 1 BLISTER PACK	3 blister pack	2019-02-01	0000-00-00	No	No	Current
53002-2304-6	53002230406	6 BLISTER PACK in 1 POUCH (53002-2304-6) > 1 KIT in 1 BLISTER PACK	6 blister pack	2019-02-01	0000-00-00	No	No	Current