Package 51672-1300-9

Brand: ammonium lactate

Generic: ammonium lactate
NDC Package

Package Facts

Identity

Package NDC 51672-1300-9
Digits Only 5167213009
Product NDC 51672-1300
Description

400 g in 1 BOTTLE, PLASTIC (51672-1300-9)

Marketing

Marketing Status
Marketed Since 2004-05-28
Brand ammonium lactate
Generic ammonium lactate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "38e594a2-48af-5554-e063-6294a90a376e", "openfda": {"nui": ["N0000175842", "M0010745"], "upc": ["0351672130053"], "unii": ["67M901L9NQ"], "rxcui": ["197362"], "spl_set_id": ["8bb09bb3-5bbc-489d-96c1-ae97cb58381e"], "pharm_class_cs": ["Hydroxy Acids [CS]"], "pharm_class_epc": ["alpha-Hydroxy Acid [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "225 g in 1 BOTTLE, PLASTIC (51672-1300-5)", "package_ndc": "51672-1300-5", "marketing_start_date": "20040528"}, {"sample": false, "description": "400 g in 1 BOTTLE, PLASTIC (51672-1300-9)", "package_ndc": "51672-1300-9", "marketing_start_date": "20040528"}], "brand_name": "Ammonium Lactate", "product_id": "51672-1300_38e594a2-48af-5554-e063-6294a90a376e", "dosage_form": "LOTION", "pharm_class": ["Acidifying Activity [MoA]"], "product_ndc": "51672-1300", "generic_name": "Ammonium Lactate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ammonium Lactate", "active_ingredients": [{"name": "AMMONIUM LACTATE", "strength": "120 mg/g"}], "application_number": "ANDA076216", "marketing_category": "ANDA", "marketing_start_date": "20040528", "listing_expiration_date": "20261231"}