Phentermine Hydrochloride
- Product NDC
- 70518-2278
- 11-digit product format
- 705182278
- Labeler code
- 70518
- Product ID
- 70518-2278_d6a67012-7bf0-68f3-e053-2995a90a140e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203068
- Marketing category
- ANDA
- Marketing start
- 2019-08-23
- Marketing end
- 0000-00-00
- Substance
- PHENTERMINE HYDROCHLORIDE
- Active strength
- 38 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
- 2023-12-31
- 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 |
|---|
| 70518-2278-0 | 70518227800 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-2278-0) | 30 tablet | 2019-08-23 | 0000-00-00 | No | No | Current |
| 70518-2278-1 | 70518227801 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-2278-1) | 100 tablet | 2020-09-18 | 0000-00-00 | No | No | Current |