Megestrol Acetate
- Product NDC
- 81646-120
- 11-digit product format
- 816460120
- Labeler code
- 81646
- Product ID
- 81646-120_88bf6275-da14-42a9-9f91-9c297021e1d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Megestrol Acetate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- PINNACLE PHARMA LLC
- Application
- ANDA075671
- Marketing category
- ANDA
- Marketing start
- 2001-03-01
- Marketing end
- 0000-00-00
- Substance
- MEGESTROL ACETATE
- Active strength
- 40 mg/mL
- Pharmacologic classes
- Progesterone Congeners [CS],Progestin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81646-120-10 | Megestrol Acetate | 10 mL in 1 CUP, UNIT-DOSE | SUSPENSION | 10 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81646-120 | MEGESTROL ACETATE SUSPENSION [PINNACLE PHARMA LLC] | 1 | Legacy NDC, 1 package rows | 20210710_904d8eef-194c-4802-9fe0-a4ac999b5002.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81646-120-10 | 81646012010 | 10 mL in 1 CUP, UNIT-DOSE (81646-120-10) | 10 ml | 2001-07-25 | 0000-00-00 | No | No | Current |