LOMAIRA
- Product NDC
- 63629-7874
- 11-digit product format
- 636297874
- Labeler code
- 63629
- Product ID
- 63629-7874_05b5a6a3-9edc-4f9f-8b09-7a002fe6c387
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203495
- Marketing category
- ANDA
- Marketing start
- 2016-09-12
- Marketing end
- 0000-00-00
- Substance
- PHENTERMINE HYDROCHLORIDE
- Active strength
- 8 mg/1
- Pharmacologic classes
- Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63629-7874-1 | 63629787401 | 30 TABLET in 1 BOTTLE (63629-7874-1) | 30 tablet | 2018-12-20 | 0000-00-00 | No | No | Current |
| 63629-7874-2 | 63629787402 | 60 TABLET in 1 BOTTLE (63629-7874-2) | 60 tablet | 2018-12-20 | 0000-00-00 | No | No | Current |
| 63629-7874-3 | 63629787403 | 90 TABLET in 1 BOTTLE (63629-7874-3) | 90 tablet | 2018-12-20 | 0000-00-00 | No | No | Current |