Stendra
- Product NDC
- 72384-752
- 11-digit product format
- 723840752
- Labeler code
- 72384
- Product ID
- 72384-752_02c03667-4518-4b43-ae10-f915132a0224
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- avanafil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Metuchen Pharmaceuticals, LLC
- Application
- NDA202276
- Marketing category
- NDA
- Marketing start
- 2013-12-27
- Marketing end
- 0000-00-00
- Substance
- AVANAFIL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 72384-752-01 | Stendra | 1 in 1 BLISTER PACK | TABLET | 1 | | 7 |
| 72384-752-30 | Stendra | 30 in 1 BOTTLE | TABLET | 30 | | 7 |
| 72384-752-99 | Stendra | 6 in 1 CARTON | TABLET | 6 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72384-752 | STENDRA (AVANAFIL) TABLET [METUCHEN PHARMACEUTICALS, LLC] | 7 | Legacy NDC, 3 package rows | 20240724_fa7d93e3-b69b-4e02-8146-89760cd8e9d6.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 |
|---|
| 72384-752-01 | 72384075201 | 1 in 1 BLISTER PACK | | | | | | Historical |
| 72384-752-30 | 72384075230 | 30 TABLET in 1 BOTTLE (72384-752-30) | 30 tablet | 2013-12-27 | 0000-00-00 | No | No | Current |
| 72384-752-99 | 72384075299 | 6 BLISTER PACK in 1 CARTON (72384-752-99) > 1 TABLET in 1 BLISTER PACK (72384-752-01) | 6 blister pack | 2020-08-10 | 0000-00-00 | Yes | No | Current |