Para Grass Pollen

Product NDC
36987-2353
11-digit product format
369872353
Labeler code
36987
Product ID
36987-2353_c4e39aa1-65b2-4426-a5ac-7e6ad761d7b8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Para Grass Pollen
Dosage form
INJECTION, SOLUTION
Route
INTRADERMAL; SUBCUTANEOUS
Labeler
Nelco Laboratories, Inc.
Application
BLA102192
Marketing category
BLA
Marketing start
1972-08-29
Marketing end
0000-00-00
Substance
UROCHLOA MUTICA POLLEN
Active strength
0 g/mL
Pharmacologic classes
Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
36987-2353-1Para Grass Pollen5 mL in 1 VIAL, MULTI-DOSEINJECTION, SOLUTION52
36987-2353-2Para Grass Pollen10 mL in 1 VIAL, MULTI-DOSEINJECTION, SOLUTION102
36987-2353-3Para Grass Pollen30 mL in 1 VIAL, MULTI-DOSEINJECTION, SOLUTION302
36987-2353-4Para Grass Pollen50 mL in 1 VIAL, MULTI-DOSEINJECTION, SOLUTION502

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
36987-2353PARA GRASS POLLEN INJECTION, SOLUTION [NELCO LABORATORIES, INC.]2Legacy NDC, 4 package rows20100107_0d4d9116-be72-4a23-8a60-8fed756e7c35.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
894753para grass pollen extract 50 MG/ML Injectable SolutionPSN0d4d9116-be72-4a23-8a60-8fed756e7c352
894753para grass pollen extract 50 MG/ML Injectable SolutionSCD0d4d9116-be72-4a23-8a60-8fed756e7c352
894753Urochloa mutica pollen extract 0.05 GM/ML Injectable SolutionSY0d4d9116-be72-4a23-8a60-8fed756e7c352
894753Urochloa mutica pollen extract 50 MG/ML Injectable SolutionSY0d4d9116-be72-4a23-8a60-8fed756e7c352

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
36987-2353-1369872353015 mL in 1 VIAL, MULTI-DOSE5 mlHistorical
36987-2353-23698723530210 mL in 1 VIAL, MULTI-DOSE10 mlHistorical
36987-2353-33698723530330 mL in 1 VIAL, MULTI-DOSE30 mlHistorical
36987-2353-43698723530450 mL in 1 VIAL, MULTI-DOSE50 mlHistorical