charlotte 24fe

Generic: norethindrone acetate and ethinyl estradiol and ferrous fumarate

Labeler: glenmark pharmaceuticals inc., usa
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug 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
Glenmark Pharmaceuticals Inc., USA

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
259176 1426288 1426600 2280761
UPC
0368462852293

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 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
source: label
Packaging
  • 3 BLISTER PACK in 1 CARTON (68462-852-29) / 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": "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"}