Grain Mill Dust is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Antigen Laboratories, Inc.. The primary component is Grain Mill Dust.
Product ID | 49288-0171_a1f5af98-9952-4103-a728-433b94a14e0a |
NDC | 49288-0171 |
Product Type | Human Prescription Drug |
Proprietary Name | Grain Mill Dust |
Generic Name | Grain Mill Dust |
Dosage Form | Injection, Solution |
Route of Administration | INTRADERMAL; SUBCUTANEOUS |
Marketing Start Date | 1974-03-23 |
Marketing Category | BLA / BLA |
Application Number | BLA102223 |
Labeler Name | Antigen Laboratories, Inc. |
Substance Name | GRAIN MILL DUST |
Active Ingredient Strength | 0 g/mL |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 1974-03-23 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | BLA |
Application Number | BLA102223 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1974-03-23 |
Inactivation Date | 2019-10-21 |
Marketing Category | BLA |
Application Number | BLA102223 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1974-03-23 |
Inactivation Date | 2019-10-21 |
Marketing Category | BLA |
Application Number | BLA102223 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1974-03-23 |
Inactivation Date | 2019-10-21 |
Marketing Category | BLA |
Application Number | BLA102223 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1974-03-23 |
Inactivation Date | 2019-10-21 |
Marketing Category | BLA |
Application Number | BLA102223 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1974-03-23 |
Inactivation Date | 2019-10-21 |
Ingredient | Strength |
---|---|
GRAIN MILL DUST | .02 g/mL |
SPL SET ID: | 0aa8cf4a-c9f7-4a4c-8e0f-beae3831b718 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |