jaimiess

Generic: levonorgestrel / ethinyl estradiol and ethinyl estradiol

Labeler: xiromed, llc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name jaimiess
Generic Name levonorgestrel / ethinyl estradiol and ethinyl estradiol
Labeler xiromed, llc.
Dosage Form KIT
Manufacturer
Xiromed, LLC.

Identifiers & Regulatory

Product NDC 70700-123
Product ID 70700-123_5f63fa1c-5741-b43e-4872-9b5f7c7afcae
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203770
Listing Expiration 2026-12-31
Marketing Start 2018-01-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70700123
Hyphenated Format 70700-123

Supplemental Identifiers

RxCUI
238019 248310 749761 2001751
UPC
0370700123874

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name jaimiess (source: ndc)
Generic Name levonorgestrel / ethinyl estradiol and ethinyl estradiol (source: ndc)
Application Number ANDA203770 (source: ndc)

Resolved Composition

Strengths
  • 0.15 mg
  • 0.03 mg
  • 0.01 mg
source: label
Packaging
  • 1 BLISTER PACK in 1 BOX (70700-123-87) / 1 KIT in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "5f63fa1c-5741-b43e-4872-9b5f7c7afcae", "openfda": {"upc": ["0370700123874"], "rxcui": ["238019", "248310", "749761", "2001751"], "spl_set_id": ["7fe3a0d4-533f-0bdf-e60a-20c69bdf79fc"], "manufacturer_name": ["Xiromed, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 BOX (70700-123-87)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "70700-123-87", "marketing_start_date": "20180101"}], "brand_name": "JAIMIESS", "product_id": "70700-123_5f63fa1c-5741-b43e-4872-9b5f7c7afcae", "dosage_form": "KIT", "product_ndc": "70700-123", "generic_name": "levonorgestrel / ethinyl estradiol and ethinyl estradiol", "labeler_name": "Xiromed, LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "JAIMIESS", "application_number": "ANDA203770", "marketing_category": "ANDA", "marketing_start_date": "20180101", "listing_expiration_date": "20261231"}