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 |
|---|---|---|---|---|---|---|
| Senna S | DOCUSATE SODIUM, SENNOSIDES | Walgreens | 765bfd9b-7a21-4315-9add-cf13007722d5 | 2025-10-31 | Warnings | F05Q2T2JA0 |
| Gentle Stool Softener | DOCUSATE SODIUM | WALGREEN COMPANY | 71b15339-2585-4fae-8445-6fbb4f0a378e | 2025-10-31 | Warnings | F05Q2T2JA0 |
| Stool Softener Laxative | DOCUSATE SODIUM | Major Pharmaceuticals | 97561cd4-63d9-44c2-a3a3-ec668a09a4ed | 2025-10-31 | Warnings | F05Q2T2JA0 |
| Stool Softener Laxative | DOCUSATE SODIUM, SENNOSIDES | Family Dollar (FAMILY WELLNESS) | 1eee3ed5-09f7-44a9-abc5-98336e493fe8 | 2025-10-30 | Warnings | F05Q2T2JA0 |
| SENNA WITH DOCUSATE SODIUM | DOCUSATE SODIUM AND SENNOSIDES | HHH Pharmaceuticals | 2bbb1b99-d43c-40a3-bc53-e18e8394c318 | 2025-10-08 | Warnings | F05Q2T2JA0 |
| Stool Softener | DOCUSATE SODIUM | Preferred Pharmaceuticals Inc. | 1d9fa4b9-3ec2-4ea2-a05a-ca46cc529167 | 2025-10-01 | Warnings | F05Q2T2JA0 |
| Stimulant Laxative Plus Stool Softener | DOCUSATE SODIUM 50 MG AND SENNOSIDES 8.6 MG | Bryant Ranch Prepack | 12f613e4-c919-4cc4-a445-eb30039ae45f | 2025-09-18 | Warnings | F05Q2T2JA0 |
| Stool Softener | DOCUSATE SODIUM | BJWC (Berkley & Jensen / BJ's) | 330758d2-fc1a-50ce-e063-6294a90a7db1 | 2025-08-19 | Warnings | F05Q2T2JA0 |
| Sennosides and Docusate Sodium | SENNOSIDES AND DOCUSATE SODIUM | American Health Packaging | 4b84d5d7-43cf-47bb-af59-088550c3a0bc | 2025-08-12 | Warnings | F05Q2T2JA0 |
| Stool Softener Laxative | DOCUSATE SODIUM | Good Sense (Geiss, Destin & Dunn, Inc.) | 8066a52d-e683-47c1-905c-290d2d427acf | 2025-08-12 | Warnings | F05Q2T2JA0 |
| Prolaxa | DOCUSATE SODIUM 250MG | Advanced Rx of Tennessee, LLC | 3ba0c0d9-9e6f-a2e6-e063-6394a90a202d | 2025-08-05 | Warnings | F05Q2T2JA0 |
| Dulcolax Stool Softener | DOCUSATE SODIUM | Chattem, Inc. | 86cb7102-3585-4757-9c37-5bf9776bbe63 | 2025-08-01 | Warnings | F05Q2T2JA0 |
| Docu Liquid | DOCUSATE SODIUM | ATLANTIC BIOLOGICALS CORP. | f4ed0721-3be9-4108-a6c9-dbbe115249e9 | 2025-07-31 | Warnings | F05Q2T2JA0 |
| Senna-S | DOCUSATE SODIUM, SENNOSIDES | Granulation Technology, Inc. | f36c509e-b93b-4d7f-a18a-41e585369a15 | 2025-07-30 | Warnings | F05Q2T2JA0 |
| Enemeez Kids | DOCUSATE SODIUM | Quest Products LLC | f1602ba4-ad02-2936-e053-2995a90a27f2 | 2025-07-15 | Warnings | F05Q2T2JA0 |
| Gencare-Senna-S Softgel | SENNOSIDES 8.6 MG AND DOCUSATE SODIUM 50 MG | Pioneer Life Sciences, LLC | e60b520a-8c7e-40cd-b829-e4c2d7904f61 | 2025-06-30 | Warnings | F05Q2T2JA0 |
| Stimulant Laxative Plus Stool Softener | DOCUSATE SODIUM 50 MG AND SENNOSIDES 8.6 MG | ATLANTIC BIOLOGICALS CORP. | 4c02fcec-6bb7-4497-96c5-0d809209dd17 | 2025-06-27 | Warnings | F05Q2T2JA0 |
| Stool Softener Extra Strength | DOCUSATE SODIUM | Chain Drug Consortium, LLC | 550000ba-0d6d-4666-8461-f591c14478b1 | 2025-06-27 | Warnings | F05Q2T2JA0 |
| Stool Softener Laxative | DOCUSATE SODIUM | Chain Drug Consortium, LLC | 09449649-fd57-4446-8264-6c3bdd6621d0 | 2025-06-27 | Warnings | F05Q2T2JA0 |
| Stool Softener Laxative | DOCUSATE SODIUM | TARGET CORPORATION | 28fce2e2-2101-df88-e063-6394a90aa3de | 2025-06-25 | Warnings | F05Q2T2JA0 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.