jaimiess
Generic: levonorgestrel / ethinyl estradiol and ethinyl estradiol
Labeler: xiromed, llc.Drug Facts
Product Profile
Brand Name
jaimiess
Generic Name
levonorgestrel / ethinyl estradiol and ethinyl estradiol
Labeler
xiromed, llc.
Dosage Form
KIT
Manufacturer
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
UPC
Packaging Origin
Original Packager
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
Packaging
- 1 BLISTER PACK in 1 BOX (70700-123-87) / 1 KIT in 1 BLISTER PACK
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"}