Package 68462-849-29

{"spl_id": "920756d5-a617-404c-968d-ccf58740fa1e", "openfda": {"upc": ["0368462849842"], "rxcui": ["1421459", "1421460", "1421461"], "spl_set_id": ["3e608414-5e64-4c69-a9e0-365904cf7df8"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 CARTON in 1 BOX (68462-849-29)  / 1 BLISTER PACK in 1 CARTON (68462-849-84)  / 1 KIT in 1 BLISTER PACK *  24 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (68462-821-40)  *  4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (68462-822-40)", "package_ndc": "68462-849-29", "marketing_start_date": "20220727"}], "brand_name": "Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate", "product_id": "68462-849_920756d5-a617-404c-968d-ccf58740fa1e", "dosage_form": "KIT", "product_ndc": "68462-849", "generic_name": "Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate", "application_number": "ANDA213418", "marketing_category": "ANDA", "marketing_start_date": "20220727", "listing_expiration_date": "20271231"}