Package 70518-2800-0

Brand: carisoprodol

Generic: carisoprodol
NDC Package

Package Facts

Identity

Package NDC 70518-2800-0
Digits Only 7051828000
Product NDC 70518-2800
Description

60 TABLET in 1 BOTTLE, PLASTIC (70518-2800-0)

Marketing

Marketing Status
Marketed Since 2020-06-25
Brand carisoprodol
Generic carisoprodol
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a909d2e-9a68-3c6b-e063-6294a90af0cb", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["21925K482H"], "rxcui": ["197446"], "spl_set_id": ["b83f7fd1-11e3-4e94-ae53-4637e892b372"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (70518-2800-0)", "package_ndc": "70518-2800-0", "marketing_start_date": "20200625"}], "brand_name": "Carisoprodol", "product_id": "70518-2800_4a909d2e-9a68-3c6b-e063-6294a90af0cb", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70518-2800", "dea_schedule": "CIV", "generic_name": "Carisoprodol", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Carisoprodol", "active_ingredients": [{"name": "CARISOPRODOL", "strength": "350 mg/1"}], "application_number": "ANDA040188", "marketing_category": "ANDA", "marketing_start_date": "20200625", "listing_expiration_date": "20271231"}