Desoxyn
- Product NDC
- 70868-820
- 11-digit product format
- 708680820
- Labeler code
- 70868
- Product ID
- 70868-820_e2081a41-c007-4a9c-ae50-af4620a51276
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methamphetamine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Key Therapeutics
- Application
- NDA005378
- Marketing category
- NDA
- Marketing start
- 2022-09-01
- Marketing end
- 0000-00-00
- Substance
- METHAMPHETAMINE HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Amphetamine Anorectic [EPC], Amphetamines [CS], Appetite Suppression [PE], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Increased Sympathetic Activity [PE]
- DEA schedule
- CII
- 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 |
|---|
| 70868-820-05 | 70868082005 | 100 TABLET in 1 BOTTLE (70868-820-05) | 100 tablet | 2022-09-01 | 0000-00-00 | No | No | Current |