Loestrin 1/20 21 Day Pack

RxCUI: 1358781
RxNorm name: Loestrin 1/20 21 Day Pack
Display name: Loestrin 1/20 21 Day Pack
Full name: Loestrin 1/20 21 Day Pack
Term type: SY
Status: DailyMed mapping
Updated: 2026-06-04 23:39:27

RxNav Current And Historical NDCs#

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UNII Substances#

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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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Loestrin Fe 28 Day	NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE	Teva Women's Health LLC	f29ebcb5-7e65-4092-bfaa-f5ec026fc255	2025-02-20	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 1358781

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 1 matching rows.

Set ID, RxNorm mappings, Terms table
Set ID	RxNorm mappings	Terms	SPL version	Label	Effective
f29ebcb5-7e65-4092-bfaa-f5ec026fc255	{21 (ethinyl estradiol 0.02 MG / norethindrone acetate 1 MG Oral Tablet) } Pack [Loestrin 1/20 21 Day] [BPCK] · LOESTRIN 1/20 21 Day Pack [PSN] · Loestrin 1/20 21 Day Pack [SY]	3	12	LOESTRIN ® 21 Day (norethindrone acetate and ethinyl estradiol tablets, USP) LOESTRIN ® Fe 28 Day (norethindrone acetate and ethinyl estradiol tablets, USP and ferrous fumarate tablets) Ferrous fumarate tablets are not USP for dissolution and assay.	20250220