NDC 68084-964-95 - Propylthiouracil
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 68084-964
- Requested NDC
- 68084-964-95
- Package NDCs from labels
- 68084-964-95, 68084-964-25
- Manufacturer
- American Health Packaging
- Effective date
- 2026-08-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Propylthiouracil - American Health Packaging | American Health Packaging | 2026-08-27 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68084-964-25 | Propylthiouracil | 30 in 1 BOX, UNIT-DOSE | TABLET | 30 | 6 | |
| 68084-964-95 | Propylthiouracil | 1 in 1 BLISTER PACK | TABLET | 1 | 6 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 68084-964-25 | EA - Each | 68084-964 | 090b7279-df0b-4fa8-8733-5703f698259b | 1 | 2015-11-12 |
| 68084-964-95 | EA - Each | 68084-964 | ad1ba66a-b99e-49f2-9006-51412d70143e | 1 | 2015-11-12 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| PROPYLTHIOURACIL | ACTIVE INGREDIENT | 721M9407IY | PROPYLTHIOURACIL TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| PROPYLTHIOURACIL | ACTIVE MOIETY | 721M9407IY | PROPYLTHIOURACIL TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | PROPYLTHIOURACIL TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| DOCUSATE SODIUM | INACTIVE INGREDIENT | F05Q2T2JA0 | PROPYLTHIOURACIL TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | PROPYLTHIOURACIL TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| SODIUM BENZOATE | INACTIVE INGREDIENT | OJ245FE5EU | PROPYLTHIOURACIL TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| SODIUM GLYCOLATE | INACTIVE INGREDIENT | B75E535IMI | PROPYLTHIOURACIL TABLET [AMERICAN HEALTH PACKAGING] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | PROPYLTHIOURACIL TABLET [AMERICAN HEALTH PACKAGING] | 1 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| ENEMEEZ | DOCUSATE SODIUM | Quest Products, LLC | 0b06445d-0839-497e-bdff-e0fe224a7738 | 2026-06-30 | Warnings | F05Q2T2JA0 |
| ENEMEEZ Plus | DOCUSATE SODIUM AND BENZOCAINE | Quest Products, LLC | 1670ca59-7275-4ac6-bef4-674a7b24c7b3 | 2026-06-30 | Warnings | F05Q2T2JA0 |
| Stool Softener Laxative | DOCUSATE SODIUM | ATLANTIC BIOLOGICALS CORP. | c1f588d0-4600-4b97-b2d3-2c08ac351e07 | 2026-06-30 | Warnings | F05Q2T2JA0 |
| Docusate Sodium | DOCUSATE SODIUM | American Health Packaging | be7cab51-ce7e-465d-95db-083e69288cfd | 2026-06-25 | Warnings | F05Q2T2JA0 |
| STOOL SOFTENER | DOCUSATE SODIUM | Geri-Care Pharmaceuticals, Corp | 3ec42148-6786-22f2-e054-00144ff8d46c | 2026-06-18 | Warnings | F05Q2T2JA0 |
| Docusate Sodium | DOCUSATE SODIUM | PD-Rx Pharmaceuticals, Inc. | 66ca7a94-378b-4476-8060-d9c6f82f57fc | 2026-06-12 | Warnings | F05Q2T2JA0 |
| Stool Softener Laxative | DOCUSATE SODIUM | Care One (Retail Business Services, LLC.) | 16691fd4-cdf3-41d4-b851-5fa148a05468 | 2026-06-08 | Warnings | F05Q2T2JA0 |
| Senna S | SENNOSIDES AND DOCUSATE SODIUM | Medline Industries, LP | 6cd22881-db60-9045-e053-2991aa0ae08a | 2026-06-04 | Warnings | F05Q2T2JA0 |
| Stool Softener | DOCUSATE SODIUM | NuCare Pharmaceuticals, Inc. | 53727f3a-914c-0e2c-e063-6394a90a3886 | 2026-06-04 | Warnings | F05Q2T2JA0 |
| Stool Softener Laxative | DOCUSATE SODIUM | CVS Pharmacy | 9983095a-6ef4-4ad7-acc5-e34221fb7c63 | 2026-05-20 | Warnings | F05Q2T2JA0 |
| Stool Softener Laxative | DOCUSATE SODIUM | CVS PHARMACY, INC | 056ec3cf-edcf-4a9a-8cfa-7cf9c4a9a138 | 2026-05-20 | Warnings | F05Q2T2JA0 |
| Sennosides and Docusate Sodium | SENNOSIDES AND DOCUSATE SODIUM | Cardinal Health 107, LLC | 40385b89-a855-4ca2-992a-df5eb677be15 | 2026-05-15 | Warnings | F05Q2T2JA0 |
| Docusate Sodium - Stool Softener Laxative | DOCUSATE SODIUM | Major Pharmaceuticals | cc8d1556-f108-4166-837c-48f81152877e | 2026-05-12 | Warnings | F05Q2T2JA0 |
| Docusate Sodium | DOCUSATE SODIUM | Forreal Pharmaceuticals, LLC | 118dccb7-5df2-432d-b7d3-37b3f1ade0aa | 2026-05-07 | Warnings | F05Q2T2JA0 |
| Docusate Sodium | DOCUSATE SODIUM | Cardinal Health 107, LLC | ee14dfe2-405f-493a-a774-ce1b01d05dd4 | 2026-05-05 | Warnings | F05Q2T2JA0 |
| Sennosides, Docusate Sodium | SENNOSIDES, DOCUSATE SODIUM | Cardinal Health 107, LLC | 1a21b07a-263c-41a4-ba0c-ad2dc5a295d7 | 2026-05-05 | Warnings | F05Q2T2JA0 |
| Docusate Sodium and Sennosides | DOCUSATE SODIUM AND SENNOSIDES | SOFTGEL HEALTHCARE PRIVATE LIMITED | 4842a767-bb12-9d85-e063-6294a90a19b5 | 2026-04-27 | Warnings | F05Q2T2JA0 |
| Stool Softener Laxative | DOCUSATE SODIUM | Publix Supermarkets, Inc. | ed50555f-b105-45c8-9dc4-1bd4d233a1e3 | 2026-04-23 | Warnings | F05Q2T2JA0 |
| Caldesene Baby | STARCH, CORN AND ZINC OXIDE | Insight Pharmaceuticals LLC | 9f12dee2-7afa-45e9-a729-0fd42bb77715 | 2026-04-22 | Warnings | O8232NY3SJ |
| Caldesene Medicated Protecting | CORNSTARCH AND ZINC OXIDE | Insight Pharmaceuticals LLC | ffc92a0f-a7cf-4a46-b2f1-089df2bbb96b | 2026-04-22 | Warnings | O8232NY3SJ |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.