Package 0641-6135-25

Brand: prochlorperazine edisylate

Generic: prochlorperazine edisylate
NDC Package

Package Facts

Identity

Package NDC 0641-6135-25
Digits Only 0641613525
Product NDC 0641-6135
Product ID 0641-6135_6ffbbb71-5711-43b7-beb5-5ccfb6128cb5
Description

25 VIAL in 1 CARTON (0641-6135-25) / 2 mL in 1 VIAL (0641-6135-01)

Marketing

Marketing Status
Marketed Since 1989-08-29
Brand prochlorperazine edisylate
Generic prochlorperazine edisylate
Sample Package No

Linked Drug Pages (1)

Prochlorperazine Edisylate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "6ffbbb71-5711-43b7-beb5-5ccfb6128cb5", "openfda": {"unii": ["PG20W5VQZS"], "rxcui": ["314192"], "spl_set_id": ["baf59816-7577-4652-b065-fb6de9e54569"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0641-6135-25)  / 2 mL in 1 VIAL (0641-6135-01)", "package_ndc": "0641-6135-25", "marketing_start_date": "19890829"}], "brand_name": "Prochlorperazine Edisylate", "product_id": "0641-6135_6ffbbb71-5711-43b7-beb5-5ccfb6128cb5", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0641-6135", "generic_name": "Prochlorperazine Edisylate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Edisylate", "active_ingredients": [{"name": "PROCHLORPERAZINE EDISYLATE", "strength": "5 mg/mL"}], "application_number": "ANDA089903", "marketing_category": "ANDA", "marketing_start_date": "19890829", "listing_expiration_date": "20261231"}