NDC 36987-1607

Okra

Okra

Okra is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Nelco Laboratories, Inc.. The primary component is Okra.

• Product ID: 36987-1607_c9d2ad91-0541-4504-a528-c0cc93a99e4e
• NDC: 36987-1607
• Product Type: Human Prescription Drug
• Proprietary Name: Okra
• Generic Name: Okra
• Dosage Form: Injection, Solution
• Route of Administration: INTRADERMAL; SUBCUTANEOUS
• Marketing Start Date: 1972-08-29
• Marketing Category: BLA / BLA
• Application Number: BLA102192
• Labeler Name: Nelco Laboratories, Inc.
• Substance Name: OKRA
• 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]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 36987-1607-2

10 mL in 1 VIAL, MULTI-DOSE (36987-1607-2)

• Marketing Start Date: 1972-08-29
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 36987-1607-4 [36987160704]

Okra INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

NDC 36987-1607-2 [36987160702]

Okra INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

NDC 36987-1607-3 [36987160703]

Okra INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

NDC 36987-1607-1 [36987160701]

Okra INJECTION, SOLUTION

• Marketing Category: BLA
• Application Number: BLA102192
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1972-08-29
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
OKRA	.05 g/mL

OpenFDA Data

• SPL SET ID: 9cf0d617-467d-461f-b6d3-d2d926982bb7
• Manufacturer:
  • Nelco Laboratories, Inc.
• UNII:
  • CFE1S8DYWD
  • AEE24M3MQ9
  • 8DS6G120HJ
  • GW0W1Y9I97
  • 3RT3536DHY
  • 44IDY6DTKX
  • J7I2T6IV1N
  • 112YH1ZMX2
  • M9WGG9Z9GK
  • RCU76P419D
  • B423VGH5S9
  • 0N8672707O
  • C5529G5JPQ
  • 0R4AQI398X
  • 65KD9TD4C3
  • Z4KHF2C175
  • V1V998DC17
  • TGD87RII2U
  • KH3E3096OO
  • M29DW54Q9E
  • 6HD2W46UEG
  • N9D69B2Q7Y
  • 8QF5D5H6UH
  • K5877MW0LE
  • 3SW678MX72
  • M98C8416QO
  • L2V28YP49S
  • 5EVU04N5QU
  • 54C8E6W6JY
  • 2ZN8DWC0YF
  • 58FMD0Q0EV
  • 6815CPT6ZJ
  • I629I3NR86
  • XKR79OET1K
  • SDS87L369F
  • 492225Q21H
  • 3OKE88I3QG
  • 4J4DOU3HEK
  • YY7C30VXJT
  • 786YV7B602
  • 5PO6NN3RRJ
  • W5K7RAS4VK
  • K48IKT5321
  • 978D8U419H
  • Y5432RGW8N
  • H3O7QI5HY7
  • 6WO75C6WVB
  • 4F3W47PLBE
  • Z38C7FBM49
  • 01G73H6H83
  • 1V3SHR7QB7
  • 24RS0A988O
  • 0E5AT8T16U
  • I5GZG55B36
  • 6L966A1IMR
  • Q74T35078H
  • 58RXI817UT
  • Z1EJP3037Z
  • 4N14V5R27W
  • KHX46H31F8
  • 3Z252A2K9G
  • X72Z47861V
  • G280W4MW6E
  • N91637DNW9
  • 5PWM7YLI7R
  • W4X7H8GYFM
  • 253RUG1X1A
  • 51ME2L7STL
  • 231473QB6R
  • O82C39RR8C
  • L7HT8F1ZOD
  • KM66971LVF
  • 61ZBX54883
  • N487KM8COK
  • Y05PC4JZRH
  • 71ES77LGJC
  • Z6J799EAJK
  • 67M3EQ6BE1
  • 2M6QWV94OC
  • 3H5U5CX7KO
  • 138LUT2DWV
  • L56Z1JK48B
  • 269CJD5GZ9
  • W2FH8O2BBE
  • 1L29G6428X
  • N0Y68724R3
  • 86R5J6D01D
  • UOI4FT57BZ
  • QE1QX6B99R
  • 8A6OMU3I8L
  • 4AJZ4765R9
  • 5S29HWU6QB
  • GH42T47V24
  • F14P91GB5F
  • 4J2I0SN84Y
  • 2A88ZO081O
  • 60RO23IR87
  • KU94FIY6JB
  • 6O38V6B52O
  • 0MVO31Q3QS
  • 8CZS546954
  • RN8P45F92A
  • 7Y1255HVXR
  • 4J2TY8Y81V
  • 9961HBA483
• RxNorm Concept Unique ID - RxCUI:
  • 891505
  • 895581
  • 901340
  • 900050
  • 895585
  • 891636
  • 899664
  • 1011630
  • 1011636
  • 967977
  • 899354
  • 899469
  • 1010882
  • 1010968
  • 978960
  • 1011407
  • 1012055
  • 905501
  • 899672
  • 1011024
  • 1012143
  • 899676
  • 901372
  • 1010957
  • 1011421
  • 899479
  • 1011030
  • 899475
  • 899473
  • 899876
  • 1011036
  • 904479
  • 1011052
  • 891640
  • 891644
  • 1010942
  • 899447
  • 1012137
  • 902747
  • 891799
  • 899451
  • 899757
  • 891655
  • 899459
  • 891614
  • 901316
  • 967985
  • 901310
  • 1010935
  • 895555
  • 904830
  • 891661
  • 899397
  • 899393
  • 899423
  • 899427
  • 899741
  • 966639
  • 899745
  • 904868
  • 899909
  • 1011046
  • 901294
  • 1010929
  • 1011063
  • 899389
  • 899381
  • 1011069
  • 904651
  • 899385
  • 899632
  • 1000013
  • 899737
  • 904487
  • 899733
  • 1010858
  • 895573
  • 895577
  • 1010850
  • 1010918
  • 1010854
  • 1010856
  • 904649
  • 904642
  • 891671
  • 899640
  • 901320
  • 1011020
  • 899401
  • 901202
  • 899483
  • 899880
  • 899727
  • 966699
  • 899886
  • 891679
  • 904533
  • 2103256
  • 891517
  • 891690
  • 1006513
  • 895591
  • 899655
  • 1011002
  • 899417
  • 899898
  • 899493
  • 899366
  • 892487
  • 899362
  • 1010700
  • 1011415
  • 899882
  • 1010974

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]

NDC Crossover Matching brand name "Okra" or generic name "Okra"

NDC	Brand Name	Generic Name
36987-1606	Okra	Okra
36987-1607	Okra	Okra
36987-1608	Okra	Okra
36987-1609	Okra	Okra