TESTOSTERONE
- Product NDC
- 71589-011
- 11-digit product format
- 715890011
- Labeler code
- 71589
- Product ID
- 71589-011_fb12ae14-fdc2-4616-bcf8-5e7305367928
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TESTOSTERONE
- Dosage form
- GEL
- Route
- TRANSDERMAL
- Labeler
- Aleor Dermaceuticals Limited
- Application
- ANDA213922
- Marketing category
- ANDA
- Marketing start
- 2021-03-12
- Marketing end
- 0000-00-00
- Substance
- TESTOSTERONE
- Active strength
- 16 mg/g
- Pharmacologic classes
- Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [CS]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71589-011-88 | 71589001188 | 1 BOTTLE, PUMP in 1 CARTON (71589-011-88) > 88 g in 1 BOTTLE, PUMP | 2021-03-12 | 0000-00-00 | No | No | Current |