NORETHINDRONE
- Product NDC
- 82804-175
- 11-digit product format
- 828040175
- Labeler code
- 82804
- Product ID
- 82804-175_bbd54f1e-2d48-4efa-a57e-7fa7b478c457
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NORETHINDRONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA091325
- Marketing category
- ANDA
- Marketing start
- 2020-11-11
- Substance
- NORETHINDRONE
- Active strength
- .35 mg/1
- Pharmacologic classes
- Progesterone Congeners [CS], Progestin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- NORETHINDRONE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NORETHINDRONE | .35 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | T18F433X4S |
| Rxcui | 198042, 748961 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82804-175-28 | NORETHINDRONE | 28 in 1 BLISTER PACK | TABLET | 28 | | 1 |
| 82804-175-28 | NORETHINDRONE | 1 in 1 BAG | TABLET | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-175-28 | 82804017528 | 1 BLISTER PACK in 1 BAG (82804-175-28) / 28 TABLET in 1 BLISTER PACK | 1 blister pack | 2020-11-11 | No | No | Current |