Testosterone
- Product NDC
- 49884-418
- 11-digit product format
- 498840418
- Labeler code
- 49884
- Product ID
- 49884-418_18413cc4-22d5-48ff-9e62-3b5909f9c22c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Testosterone
- Dosage form
- GEL
- Route
- TRANSDERMAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA076744
- Marketing category
- ANDA
- Marketing start
- 2015-09-02
- Marketing end
- 0000-00-00
- Substance
- TESTOSTERONE
- Active strength
- 25 mg/2.5g
- Pharmacologic classes
- Androgen Receptor Agonists [MoA], Androgen [EPC], Androstanes [CS]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 49884-418-72 | 49884041872 | 30 PACKET in 1 CARTON (49884-418-72) > 2.5 g in 1 PACKET (49884-418-48) | 30 packet | 2015-09-02 | 0000-00-00 | No | No | Current |