Alora
- Product NDC
- 0023-5885
- 11-digit product format
- 000235885
- Labeler code
- 0023
- Product ID
- 0023-5885_4ec6701d-54cd-4f8f-8449-02f43094950e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Estradiol
- Dosage form
- PATCH
- Route
- TRANSDERMAL
- Labeler
- Allergan, Inc.
- Application
- NDA020655
- Marketing category
- NDA
- Marketing start
- 2002-04-05
- Marketing end
- 2022-07-01
- Substance
- ESTRADIOL
- Active strength
- 0 mg/d
- Pharmacologic classes
- Estradiol Congeners [CS],Estrogen [EPC],Estrogen Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0023-5885-12 | 00023588512 | 8 POUCH in 1 BOX (0023-5885-12) > 1 PATCH in 1 POUCH > 3.5 d in 1 PATCH | 8 pouch | 2002-04-05 | 0000-00-00 | No | No | Current |