36987-3379 NDC - GREASEWOOD ()

Drug Information

No.	Package Code	Package Description
1	36987-3379-1	5 mL in 1 VIAL, MULTI-DOSE (36987-3379-1)
2	36987-3379-2	10 mL in 1 VIAL, MULTI-DOSE (36987-3379-2)
3	36987-3379-3	30 mL in 1 VIAL, MULTI-DOSE (36987-3379-3)
4	36987-3379-4	50 mL in 1 VIAL, MULTI-DOSE (36987-3379-4)

Field Name	Field Value	Definition
PRODUCT NDC	36987-3379	Name of Company corresponding to the labeler code segment of the Product NDC.
PROPRIETARY NAME	Greasewood	This is the date that the labeler indicates was the start of its marketing of the drug product.
START MARKETING DATE	8/29/1972	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BLA	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBER	BLA102192	This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAME	Nelco Laboratories, Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.