NDC 16729-035-17 - Anastrozole
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
- 16729-035
- Requested NDC
- 16729-035-17
- Package NDCs from labels
- 16729-035-10, 16729-035-15, 16729-035-16, 16729-035-17
- Manufacturer
- PD-Rx Pharmaceuticals, Inc.
- Effective date
- 2026-07-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Anastrozole - PD-Rx Pharmaceuticals, Inc. | PD-Rx Pharmaceuticals, Inc. | 2026-07-07 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM | 2026-02-14 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - Accord Healthcare Inc. | Intas Pharmaceuticals Limited | Accord Healthcare Inc. | Intas Pharmaceuticals Limited | 2026-02-11 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - REMEDYREPACK INC. | REMEDYREPACK INC. | 2025-07-07 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2025-04-03 | HUMAN PRESCRIPTION DRUG LABEL |
| ANASTROZOLE - Direct_Rx | Direct_Rx | 2025-01-22 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2024-12-26 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-08-22 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - Major Pharmaceuticals | Major Pharmaceuticals | 2024-06-26 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2024-06-20 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - A-S Medication Solutions | A-S Medication Solutions | 2024-06-05 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2024-04-05 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - REMEDYREPACK INC. | REMEDYREPACK INC. | 2023-11-29 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - Proficient Rx LP | Proficient Rx LP | 2023-05-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - Preferred Pharmaceuticals, Inc. | Preferred Pharmaceuticals, Inc. | 2020-03-03 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - Denton Pharma, Inc. DBA Northwind Pharmaceuticals | Denton Pharma, Inc. DBA Northwind Pharmaceuticals | 2020-01-08 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - medsource pharmaceuticals | medsource pharmaceuticals | 2018-12-20 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - Northwind Pharmaceuticals, LLC | Northwind Pharmaceuticals, LLC | 2014-11-10 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - Dispensing Solutions, Inc. | PSS World Medical, Inc. | Dispensing Solutions, Inc. | PSS World Medical, Inc. | 2013-10-23 | HUMAN PRESCRIPTION DRUG LABEL |
| Anastrozole - Rebel Distributors Corp | Rebel Distributors Corp | 2012-02-29 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 16729-035-10 | Anastrozole | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | 11 | |
| 16729-035-15 | Anastrozole | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | 11 | |
| 16729-035-16 | Anastrozole | 500 in 1 BOTTLE, PLASTIC | TABLET | 500 | 11 | |
| 16729-035-17 | Anastrozole | 1000 in 1 BOTTLE, PLASTIC | TABLET | 1000 | 11 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 16729-035-10 | EA - Each | 16729-035 | f3bee17f-5c8a-4f7f-9dd9-6daca91b6e62 | 1 | 2012-07-24 |
| 16729-035-15 | EA - Each | 16729-035 | 998f9f25-5ae0-40be-b774-9c3b2ee84f39 | 1 | 2013-02-13 |
| 16729-035-16 | EA - Each | 16729-035 | 1955c597-70f2-4c95-86b0-e14acf1ca10f | 1 | 2013-02-13 |
DailyMed Socrata Ingredients#
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.