Home NDC 70700-123 JAIMIESS
Product NDC 70700-123
11-digit product format 707000123
Labeler code 70700
Product ID 70700-123_99b59a89-1937-6cad-e31b-dc192f9f3891
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name levonorgestrel / ethinyl estradiol and ethinyl estradiol
Dosage form KIT
Labeler Xiromed, LLC.
Application ANDA203770
Marketing category ANDA
Marketing start 2018-01-01
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 A203770-001 JAIMIESS ETHINYL ESTRADIOL; LEVONORGESTREL 0.03MG,0.01MG;0.15MG,N/A TABLET / ORAL AB 2017-12-27
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 1 matching rows.
Application-product, TE code table Application-product TE code A203770-001 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 A203770-001 JAIMIESS 0.03MG,0.01MG;0.15MG,N/A TABLET / ORAL AB 2017-12-27 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 A203770-001 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 · 2 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base JAIMIESS
Listing expiration 2027-12-31 Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 4 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 238019 Internal RxNorm lookup 248310 Internal RxNorm lookup 749761 Internal RxNorm lookup 2001751 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70700-123-87 JAIMIESS 1 in 1 BLISTER PACK KIT 1 10 70700-123-87 JAIMIESS 1 in 1 BOX KIT 1 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70700-123 JAIMIESS (LEVONORGESTREL / ETHINYL ESTRADIOL AND ETHINYL ESTRADIOL) KIT [XIROMED, LLC.] 9 Current NDC, Legacy NDC, 2 package rows 20230928_7fe3a0d4-533f-0bdf-e60a-20c69bdf79fc.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70700-123-87 70700012387 1 BLISTER PACK in 1 BOX (70700-123-87) / 1 KIT in 1 BLISTER PACK 1 blister pack 2018-01-01 0000-00-00 No No Current