Domain created to manage non eCTD4 controlled vocabularies required to support IDMP
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HA Controlled Vocabulary
Controlled Vocabulary / Code System Name as defoined by the Health Authority
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Term
Term Description as defined by the Health Authority
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Code
Code, if any, associated with the term by the Health Authority
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Agency
Name of the issuing Health Authority (abbreviation) that maintains the term and code
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Status
Current status of the Term usage as defined by the Health Authority (e.g., Current, Retired, Deprecated)
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| SPL Combination Product Type Terminology | Type 0: Not a Combination Product |
C112160
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FDA | — |
| SPL Combination Product Type Terminology | Type 1: Convenience Kit or Co-Package |
C102834
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FDA | — |
| SPL Combination Product Type Terminology | Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.) |
C102835
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FDA | — |
| SPL Combination Product Type Terminology | Type 3: Prefilled Biologic Delivery Device/System (syringe, patch, etc.) |
C102836
|
FDA | — |
| SPL Combination Product Type Terminology | Type 4: Device Coated/Impregnated/Otherwise Combined with Drug |
C102837
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FDA | — |
| SPL Combination Product Type Terminology | Type 5: Device Coated or Otherwise Combined with Biologic |
C102838
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FDA | — |
| SPL Combination Product Type Terminology | Type 6: Drug/Biologic Combination |
C102839
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FDA | — |
| SPL Combination Product Type Terminology | Type 7: Separate Products Requiring Cross Labeling |
C102840
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FDA | — |
| SPL Combination Product Type Terminology | Type 8: Possible Combination Based on Cross Labeling of Separate Products (Temporary Type) |
C102841
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FDA | — |
| SPL Combination Product Type Terminology | Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product) |
C102842
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FDA | — |
| SPL Marketing Category Terminology | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
C101533
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FDA | — |
| SPL Marketing Category Terminology | UNAPPROVED DRUG OTHER MARKETING CATEGORY |
C73627
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FDA | — |
| SPL Marketing Category Terminology | UNAPPROVED DRUG PRODUCT MANUFACTURED EXCLUSIVELY FOR PRIVATE LABEL DISTRIBUTOR |
C95602
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FDA | — |
| SPL Marketing Category Terminology | Unapproved Drug Product Manufactured Under Contract |
C132335
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FDA | — |
| SPL Marketing Category Terminology | UNAPPROVED HOMEOPATHIC |
C73614
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FDA | — |
| SPL Marketing Category Terminology | UNAPPROVED MEDICAL GAS |
C73613
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FDA | — |
| SPL Marketing Category Terminology | UNAPPROVED VITAMIN DRUG |
C73615
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FDA | — |
| SPL Drug Route of Administration Terminology | UNASSIGNED |
C38310
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FDA | — |
| SPL Business Operation Terminology | UNITED STATES AGENT |
C73330
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FDA | — |
| SPL Drug Route of Administration Terminology | UNKNOWN |
C38311
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FDA | — |
| SPL Drug Route of Administration Terminology | URETERAL |
C38312
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FDA | — |
| SPL Drug Route of Administration Terminology | URETHRAL |
C38271
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FDA | — |
| SPL Drug Route of Administration Terminology | VAGINAL |
C38313
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FDA | — |
| SPL Pharmaceutical Dosage Form Terminology | WAFER |
C43003
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FDA | — |
| SPL Business Operation Qualifier Terminology | Warehouses human prescription drug products |
C123274
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FDA | — |
Showing 376–400 of 401 terms . Data sourced from public health authority publications and updated periodically.