Package 15631-2812-1

Brand: lachesis m

Generic: lachesis m
NDC Package

Package Facts

Identity

Package NDC 15631-2812-1
Digits Only 1563128121
Product NDC 15631-2812
Description

30 mL in 1 BOTTLE (15631-2812-1)

Marketing

Marketing Status
Marketed Since 2024-05-23
Brand lachesis m
Generic lachesis m
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1a236753-b79c-10f8-e063-6294a90ab3f9", "openfda": {"unii": ["VSW71SS07I"], "spl_set_id": ["1a2361f9-226d-0b55-e063-6394a90a083c"], "manufacturer_name": ["Rxhomeo Private Limited d.b.a. Rxhomeo, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 BOTTLE (15631-2812-0)", "package_ndc": "15631-2812-0", "marketing_start_date": "20240523"}, {"sample": false, "description": "30 mL in 1 BOTTLE (15631-2812-1)", "package_ndc": "15631-2812-1", "marketing_start_date": "20240523"}], "brand_name": "LACHESIS M", "product_id": "15631-2812_1a236753-b79c-10f8-e063-6294a90ab3f9", "dosage_form": "LIQUID", "product_ndc": "15631-2812", "generic_name": "LACHESIS M", "labeler_name": "Rxhomeo Private Limited d.b.a. Rxhomeo, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "LACHESIS M", "active_ingredients": [{"name": "LACHESIS MUTA VENOM", "strength": "8 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240523", "listing_expiration_date": "20261231"}