NDC 49288-0162

Dill Seed

Dill Seed

Dill Seed 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 Dill.

Product ID	49288-0162_1d11d7ba-8b48-401c-a02e-42b54abb4296
NDC	49288-0162
Product Type	Human Prescription Drug
Proprietary Name	Dill Seed
Generic Name	Dill Seed
Dosage Form	Injection, Solution
Route of Administration	INTRADERMAL; SUBCUTANEOUS
Marketing Start Date	1974-03-26
Marketing Category	BLA / BLA
Application Number	BLA102223
Labeler Name	Antigen Laboratories, Inc.
Substance Name	DILL
Active Ingredient Strength	0 g/mL
Pharm Classes	Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Food Additives [CS]
NDC Exclude Flag	E
Listing Certified Through	2017-12-31

Packaging

NDC 49288-0162-3

10 mL in 1 VIAL, MULTI-DOSE (49288-0162-3)

Marketing Start Date	1974-03-26
NDC Exclude Flag	N
Sample Package?	N

NDC SPL Data Element Entries

NDC 49288-0162-1 [49288016201]

Dill Seed INJECTION, SOLUTION

Marketing Category	BLA
Application Number	BLA102223
Product Type	HUMAN PRESCRIPTION DRUG
Marketing Start Date	1974-03-26
Inactivation Date	2019-10-21

NDC 49288-0162-2 [49288016202]

Dill Seed INJECTION, SOLUTION

Marketing Category	BLA
Application Number	BLA102223
Product Type	HUMAN PRESCRIPTION DRUG
Marketing Start Date	1974-03-26
Inactivation Date	2019-10-21

NDC 49288-0162-5 [49288016205]

Dill Seed INJECTION, SOLUTION

Marketing Category	BLA
Application Number	BLA102223
Product Type	HUMAN PRESCRIPTION DRUG
Marketing Start Date	1974-03-26
Inactivation Date	2019-10-21

NDC 49288-0162-3 [49288016203]

Dill Seed INJECTION, SOLUTION

Marketing Category	BLA
Application Number	BLA102223
Product Type	HUMAN PRESCRIPTION DRUG
Marketing Start Date	1974-03-26
Inactivation Date	2019-10-21

NDC 49288-0162-4 [49288016204]

Dill Seed INJECTION, SOLUTION

Marketing Category	BLA
Application Number	BLA102223
Product Type	HUMAN PRESCRIPTION DRUG
Marketing Start Date	1974-03-26
Inactivation Date	2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
DILL	.05 g/mL

OpenFDA Data

SPL SET ID:	f2adabd1-ea12-437a-a902-da240cf2a62c
Manufacturer	Antigen Laboratories, Inc.
UNII	N487KM8COK 93T4562ZI3 AEE24M3MQ9 GW0W1Y9I97 3RT3536DHY 44IDY6DTKX J7I2T6IV1N 112YH1ZMX2 M9WGG9Z9GK B423VGH5S9 0N8672707O C5529G5JPQ 0R4AQI398X Z4KHF2C175 V1V998DC17 6HD2W46UEG N9D69B2Q7Y 02WM57RXZJ 8QF5D5H6UH M98C8416QO 5EVU04N5QU 54C8E6W6JY 2ZN8DWC0YF 58FMD0Q0EV XKR79OET1K SDS87L369F 492225Q21H 3OKE88I3QG 4J4DOU3HEK YY7C30VXJT 786YV7B602 5PO6NN3RRJ W5K7RAS4VK K48IKT5321 978D8U419H H3O7QI5HY7 6WO75C6WVB 5M338IN22E Z38C7FBM49 01G73H6H83 1V3SHR7QB7 24RS0A988O Q74T35078H 58RXI817UT Z1EJP3037Z 4N14V5R27W AG9BNA51DQ KHX46H31F8 3Z252A2K9G X72Z47861V 4VBL71TY4Y 5PWM7YLI7R W4X7H8GYFM 253RUG1X1A R9N3379M4Z 231473QB6R O82C39RR8C L7HT8F1ZOD KM66971LVF CFE1S8DYWD T3PW93IB4Q Y05PC4JZRH Z6J799EAJK 67M3EQ6BE1 3H5U5CX7KO 138LUT2DWV L56Z1JK48B 24SC3U704I 269CJD5GZ9 3GOV20705G SYW0QUB89Y 1LIB31N73G N0Y68724R3 86R5J6D01D UOI4FT57BZ QE1QX6B99R 8A6OMU3I8L 4AJZ4765R9 5S29HWU6QB F14P91GB5F 4J2I0SN84Y 2A88ZO081O 6O38V6B52O 0MVO31Q3QS 8CZS546954 RN8P45F92A 4J2TY8Y81V 2U0KZP0FDW 7Y1255HVXR
RxNorm Concept Unique ID - RxCUI	901340 900050 895585 891636 899664 1011630 967977 899352 899354 899469 899358 1010882 978960 905501 899773 899672 899676 901372 899479 899475 899473 899876 904479 891724 901368 891640 891644 899447 902747 891799 899455 899451 891650 899757 891655 899459 1006513 901316 967985 901310 891661 899397 899393 899423 899427 899741 899745 904868 901306 899909 901349 901294 899493 899389 904487 904651 899385 899632 1000013 899737 901332 899733 895573 904649 904642 891671 899640 901320 899401 901206 901202 899483 899880 899727 899886 891679 899381 904533 2103256 891698 891517 891690 892320 891614 899655 899417 899898 901198 899366 899362 901194 899882

Pharmacological Class

Non-Standardized Plant Allergenic Extract [EPC]
Non-Standardized Food Allergenic Extract [EPC]
Increased Histamine Release [PE]
Cell-mediated Immunity [PE]
Allergens [CS]
Dietary Proteins [CS]
Plant Proteins [CS]
Food Additives [CS]

NDC Crossover Matching brand name "Dill Seed" or generic name "Dill Seed"

NDC	Brand Name	Generic Name
49288-0162	Dill Seed	Dill Seed
54575-388	DILL SEED	dill

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.