Megestrol Acetate
- Product NDC
- 71205-943
- 11-digit product format
- 712050943
- Labeler code
- 71205
- Product ID
- 71205-943_e9000264-858a-4fcd-af09-21460169305d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Megestrol Acetate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA203139
- Marketing category
- ANDA
- Marketing start
- 2015-03-01
- Substance
- MEGESTROL ACETATE
- Active strength
- 125 mg/mL
- Pharmacologic classes
- Progesterone Congeners [CS], Progestin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Megestrol Acetate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MEGESTROL ACETATE | 125 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | TJ2M0FR8ES |
| Rxcui | 577154 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71205-943-15 | Megestrol Acetate | 150 mL in 1 BOTTLE | SUSPENSION | 150 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-943 | MEGESTROL ACETATE SUSPENSION [PROFICIENT RX LP] | 2 | Current NDC, Legacy NDC, 1 package rows | 20220518_6342df31-afce-4deb-b992-e08e2a4b2b77.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 |
|---|
| 71205-943-15 | 71205094315 | 150 mL in 1 BOTTLE (71205-943-15) | 150 ml | 2020-11-19 | 0000-00-00 | No | No | Current |