Estropipate
- Product NDC
- 0591-0415
- 11-digit product format
- 005910415
- Labeler code
- 0591
- Product ID
- 0591-0415_fc393e85-ce9e-4647-aac8-77b231b38abf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Estropipate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA081214
- Marketing category
- ANDA
- Marketing start
- 1993-09-23
- Marketing end
- 0000-00-00
- Substance
- ESTROPIPATE
- Active strength
- 2 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0591-0415-01 | EA - Each | 0591-0415 | bc59e7ca-b073-49e8-a84f-a4073bb8b81d | 1 | 2012-07-24 |