NDC 17856-0060-2 - Megestrol Acetate
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
- 17856-0060
- Requested NDC
- 17856-0060-2
- Package NDCs from labels
- 17856-0060-1, 17856-0060-3, 17856-0060-2, 17856-0060-4
- Manufacturer
- ATLANTIC BIOLOGICALS CORP.
- Effective date
- 2026-07-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| MEGESTROL ACETATE ORAL SUSPENSION, USP | ATLANTIC BIOLOGICALS CORP. | 2026-07-09 | HUMAN PRESCRIPTION DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 17856-0060-3 | 2024-05-09 | MEGESTROL ACETATE ORAL SUSPENSION, USP |
| 17856-0060-3 | 2024-05-09 | MEGESTROL ACETATE ORAL SUSPENSION, USP |
| 17856-0060-4 | 2024-05-09 | MEGESTROL ACETATE ORAL SUSPENSION, USP |
| 17856-0060-4 | 2024-05-09 | MEGESTROL ACETATE ORAL SUSPENSION, USP |
| 17856-0060-3 | 2024-01-30 | MEGESTROL ACETATE ORAL SUSPENSION, USP |
| 17856-0060-3 | 2024-01-30 | MEGESTROL ACETATE ORAL SUSPENSION, USP |
| 17856-0060-4 | 2024-01-30 | MEGESTROL ACETATE ORAL SUSPENSION, USP |
| 17856-0060-4 | 2024-01-30 | MEGESTROL ACETATE ORAL SUSPENSION, USP |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17856-0060-1 | Megestrol Acetate | 10 mL in 1 CUP | SUSPENSION | 10 | 3 | |
| 17856-0060-2 | Megestrol Acetate | 20 mL in 1 CUP | SUSPENSION | 20 | 3 | |
| 17856-0060-3 | Megestrol Acetate | 72 in 1 BOX | SUSPENSION | 72 | 3 | |
| 17856-0060-4 | Megestrol Acetate | 50 in 1 BOX | SUSPENSION | 50 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 17856-0060 | MEGESTROL ACETATE SUSPENSION [ATLANTIC BIOLOGICALS CORP.] | 3 | Current NDC, Legacy NDC, 4 package rows | 20250524_01119031-9943-4afb-8b45-cb71682f0482.zip |
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 |
|---|---|---|---|---|---|---|
| Zenibell Snail Intensive | GLYCERIN | MISOCOS | 97747267-26f1-d06f-e053-2a95a90ab087 | 2024-07-04 | Warnings | PDC6A3C0OX |
| Fleet | DOCUSATE SODIUM | C.B. Fleet Company, Inc. | 56a7b6c5-d674-4eed-91c2-77f7d18fff32 | 2024-06-27 | Warnings | F05Q2T2JA0 |
| Stool Softener Laxative Extra Strength | DOCUSATE SODIUM | WALMART INC. (see also Equate) | 2cf6c9bf-c318-445d-9306-5675b1d424b0 | 2024-06-26 | Warnings | F05Q2T2JA0 |
| Stool Softener Laxative | DOCUSATE SODIUM | WALMART INC. (see also Equate) | d9db24b5-e3b5-47f9-b86b-bc8d70896a11 | 2024-06-26 | Warnings | F05Q2T2JA0 |
| ABREVA Rapid Pain Relief | GLYCERIN, LIDOCAINE | Haleon US Holdings LLC | 65bd242f-4c6a-436c-8ec0-7b2e0d73ed9d | 2024-06-20 | Warnings | PDC6A3C0OX |
| Stool Softener Plus Stimulant Laxative | DOCUSATE SODIUM AND SENNOSIDES | TOP CARE (Topco Associates LLC) | 3b184800-649b-45d0-9586-8055d6d7fe08 | 2024-06-20 | Warnings | F05Q2T2JA0 |
| Stool Softener | STOOL SOFTENER | Good Sense | 64266195-1b07-42c2-98a7-d76c12f74776 | 2024-06-18 | Warnings | F05Q2T2JA0 |
| Stool Softener Plus Stimulant | DOCUSATE SODIUM AND SENNOSIDES | United Natural Foods, Inc. dba UNFI | 6c8c7c46-3ded-4e89-8e16-30eeb72aa08b | 2024-06-14 | Warnings | F05Q2T2JA0 |
| Stool Softener Plus Stimulant Laxative | DOCUSATE SODIUM AND SENNOSIDES | United Natural Foods, Inc. dba UNFI | 50ca1ce2-885f-4b71-a5fb-90c2cf508ce6 | 2024-06-14 | Warnings | F05Q2T2JA0 |
| basic care stool softener | DOCUSATE SODIUM | Amazon.com Services LLC | 356a889f-ec23-4eb2-a25c-bbe609475155 | 2024-06-14 | Warnings | F05Q2T2JA0 |
| Stool Softener Laxative | DOCUSATE SODIUM | United Natural Foods, Inc. dba UNFI | 88cc2575-27a1-4514-bc41-bd1eac283814 | 2024-06-13 | Warnings | F05Q2T2JA0 |
| MegaBabe Butt Stuff Hemorrhoidal | COCOA BUTTER, GLYCERIN, LIDOCAINE, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE | MEGABABE, LLC | 01c156ff-69f9-4d5e-a9ea-abbc52d4afff | 2024-06-12 | Warnings | PDC6A3C0OX |
| Stool Softener Laxative | DOCUSATE SODIUM | TARGET Corporation | 1b7edd67-7b14-4fdd-9821-637f4b3c3a2c | 2024-06-06 | Warnings | F05Q2T2JA0 |
| Megestrol Acetate | MEGESTROL ACETATE | Golden State Medical Supply, Inc. | 19c33213-7919-208d-e063-6394a90a0f08 | 2024-05-31 | Warnings, Adverse reactions | ANDA075671 860225 TJ2M0FR8ES |
| Sodium Citrate and Citric Acid | SODIUM CITRATE AND CITRIC ACID | Chartwell RX, LLC | 525136c9-7758-437b-b57b-94b905786825 | 2024-05-31 | Adverse reactions | 2968PHW8QP 1Q73Q2JULR |
| Stool Softener Laxative | DOCUSATE SODIUM | United Natural Foods, Inc. dba UNFI | b1d903a5-1d5f-44d4-9939-a4b86e5a620d | 2024-05-23 | Warnings | F05Q2T2JA0 |
| Stool Softener | DOCUSATE SODIUM | Sam's West, Inc | b14d2495-1092-4063-869f-73a7e8c28708 | 2024-05-21 | Warnings | F05Q2T2JA0 |
| Allergies | APIS MELLIFICA, ECHINACEA, HYDRASTIS CANADENSIS, TARAXACUM OFFICINALE, ACONITUM NAPELLUS, AETHUSA CYNAPIUM, AGARICUS MUSCARIUS, ALETRIS FARINOSA, ALFALFA, ALLIUM CEPA, ALLIUM SATIVUM, AMBROSIA ARTEMISIAEFOLIA, ARSENICUM ALBUM, ARTEMISIA VULGARIS, ARUNDO MAURITANICA, AVENA SATIVA, BELLADONNA, BELLIS PERRENIS, BOVISTA, BROMIUM, BRYONIA, CAFFEINUM, CALCAREA CARBONICA, CALLUNA VULGARIS, FLOS, CAPSICUM ANNUUM, CAT HAIR, CHAMOMILLA, CHELIDONIUM MAJUS, CHENOPODIUM ANTHELMINTICUM, CINNAMOMUM | Newton Laboratories, Inc. | 9d5dea47-5103-21a3-e053-2995a90aee78 | 2024-05-20 | Warnings | C151H8M554 |
| Stool Softener Plus Stimulant Laxative | DOCUSATE SODIUM AND SENNOSIDES | Safeway, Inc. | 6bc9ea37-31b8-4a6d-9b2d-2c80bad4f30d | 2024-05-15 | Warnings | F05Q2T2JA0 |
| Stool Softener Plus Stimulant Laxative | DOCUSATE SODIUM AND SENNOSIDES | Safeway, Inc. | c0898583-4bbb-41d5-9e84-00cca823024f | 2024-05-15 | Warnings | F05Q2T2JA0 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.