NDC 16729-372-17 - Tadalafil
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
- 16729-372
- Requested NDC
- 16729-372-17
- Package NDCs from labels
- 16729-372-10, 16729-372-15, 16729-372-16, 16729-372-17
- Manufacturer
- A-S Medication Solutions
- Effective date
- 2026-08-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Tadalafil - A-S Medication Solutions | A-S Medication Solutions | 2026-08-25 | HUMAN PRESCRIPTION DRUG LABEL |
| Tadalafil - Bryant Ranch Prepack | Bryant Ranch Prepack | 2026-05-13 | HUMAN PRESCRIPTION DRUG LABEL |
| Tadalafil - Accord Healthcare Inc. | ACME GENERICS PRIVATE LIMITED | Intas Pharmaceuticals Limited | Accord Healthcare Inc. | ACME GENERICS PRIVATE LIMITED | Intas Pharmaceuticals Limited | 2026-04-16 | HUMAN PRESCRIPTION DRUG LABEL |
| Tadalafil - Preferred Pharmaceuticals Inc. | Preferred Pharmaceuticals Inc. | 2026-01-12 | HUMAN PRESCRIPTION DRUG LABEL |
| Tadalafil - Northwind Health Company, LLC | Northwind Health Company, LLC | 2026-01-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Tadalafil - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2025-02-10 | HUMAN PRESCRIPTION DRUG LABEL |
| Tadalafil - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2024-06-20 | HUMAN PRESCRIPTION DRUG LABEL |
| Tadalafil - Denton Pharma, Inc. DBA Northwind Pharmaceuticals | Denton Pharma, Inc. DBA Northwind Pharmaceuticals | 2023-01-13 | HUMAN PRESCRIPTION DRUG LABEL |
| Tadalafil - Unit Dose Services | Unit Dose Services | 2022-09-21 | HUMAN PRESCRIPTION DRUG LABEL |
| TADALAFIL - UNYTER ENTERPRISES | UNYTER ENTRPRISES | UNYTER ENTERPRISES | UNYTER ENTRPRISES | 2022-04-02 | HUMAN PRESCRIPTION DRUG LABEL |
| Tadalafil - Proficient Rx LP | Proficient Rx LP | 2022-04-01 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 16729-372-10 | Tadalafil | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 15 | |
| 16729-372-15 | Tadalafil | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 15 | |
| 16729-372-16 | Tadalafil | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | 15 | |
| 16729-372-17 | Tadalafil | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | 15 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 16729-372-10 | EA - Each | 16729-372 | 755119d4-223d-4dce-970a-1358a29290e1 | 1 | 2019-04-11 |
| 16729-372-16 | EA - Each | 16729-372 | 61cf467b-f24a-44f9-90c9-194f4a3af260 | 1 | 2020-05-08 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.