MICROGESTIN Fe 1/20
- Product NDC
- 53002-1616
- 11-digit product format
- 530021616
- Labeler code
- 53002
- Product ID
- 53002-1616_9b1e979a-4186-49de-bfe2-2bc92d745eb6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- norethindrone acetate and ethinyl estradiol and ferrous fumarate
- Dosage form
- KIT
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- NDA017354
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-08-05
- Marketing end
- 0000-00-00
- Active strength
- 0
- 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 |
|---|
| 53002-1616-1 | 53002161601 | 1 BLISTER PACK in 1 PACKAGE (53002-1616-1) > 1 KIT in 1 BLISTER PACK | 1 blister pack | 2017-09-01 | 0000-00-00 | No | No | Current |
| 53002-1616-3 | 53002161603 | 3 BLISTER PACK in 1 PACKAGE (53002-1616-3) > 1 KIT in 1 BLISTER PACK | 3 blister pack | 2017-09-01 | 0000-00-00 | No | No | Current |
| 53002-1616-6 | 53002161606 | 6 BLISTER PACK in 1 PACKAGE (53002-1616-6) > 1 KIT in 1 BLISTER PACK | 6 blister pack | 2017-09-01 | 0000-00-00 | No | No | Current |