charlotte 24fe
Generic: norethindrone acetate and ethinyl estradiol and ferrous fumarate
Labeler: glenmark pharmaceuticals inc., usaDrug Facts
Product Profile
Brand Name
charlotte 24fe
Generic Name
norethindrone acetate and ethinyl estradiol and ferrous fumarate
Labeler
glenmark pharmaceuticals inc., usa
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
68462-852
Product ID
68462-852_d5dfc9ba-16e2-4a8f-babf-b4a159785d47
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210369
Listing Expiration
2027-12-31
Marketing Start
2020-02-20
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68462852
Hyphenated Format
68462-852
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
charlotte 24fe (source: ndc)
Generic Name
norethindrone acetate and ethinyl estradiol and ferrous fumarate (source: ndc)
Application Number
ANDA210369 (source: ndc)
Resolved Composition
Strengths
- 1 mg
- 20 mcg
- 75 mg
Packaging
- 3 BLISTER PACK in 1 CARTON (68462-852-29) / 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": "d5dfc9ba-16e2-4a8f-babf-b4a159785d47", "openfda": {"upc": ["0368462852293"], "rxcui": ["259176", "1426288", "1426600", "2280761"], "spl_set_id": ["b01f8921-8844-43e6-8167-561ff03c21ef"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (68462-852-29) / 1 KIT in 1 BLISTER PACK", "package_ndc": "68462-852-29", "marketing_start_date": "20200220"}], "brand_name": "Charlotte 24Fe", "product_id": "68462-852_d5dfc9ba-16e2-4a8f-babf-b4a159785d47", "dosage_form": "KIT", "product_ndc": "68462-852", "generic_name": "norethindrone acetate and ethinyl estradiol and ferrous fumarate", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Charlotte 24Fe", "application_number": "ANDA210369", "marketing_category": "ANDA", "marketing_start_date": "20200220", "listing_expiration_date": "20271231"}