Tulana
- Product NDC
- 53002-2687
- 11-digit product format
- 530022687
- Labeler code
- 53002
- Product ID
- 53002-2687_c11dffa5-8555-436c-8c76-8caa1fe266c0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NORETHINDRONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA207304
- Marketing category
- ANDA
- Marketing start
- 2016-09-23
- Marketing end
- 0000-00-00
- Substance
- NORETHINDRONE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Progesterone Congeners [CS],Progestin [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-2687-1 | 53002268701 | 1 BLISTER PACK in 1 PACKAGE (53002-2687-1) > 28 TABLET in 1 BLISTER PACK | 1 blister pack | 2019-01-01 | 0000-00-00 | No | No | Current |
| 53002-2687-3 | 53002268703 | 1 BLISTER PACK in 1 PACKAGE (53002-2687-3) > 28 TABLET in 1 BLISTER PACK | 1 blister pack | 2019-01-01 | 0000-00-00 | No | No | Current |
| 53002-2687-6 | 53002268706 | 1 BLISTER PACK in 1 PACKAGE (53002-2687-6) > 28 TABLET in 1 BLISTER PACK | 1 blister pack | 2019-01-01 | 0000-00-00 | No | No | Current |