Phentermine Hydrochloride
- Product NDC
- 64980-190
- 11-digit product format
- 649800190
- Labeler code
- 64980
- Product ID
- 64980-190_ec6eaef8-771d-4ffb-b2d2-603691362709
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phentermine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rising Pharmaceuticals, Inc.
- Application
- ANDA091451
- Marketing category
- ANDA
- Marketing start
- 2012-09-21
- 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
- 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 |
|---|
| 64980-190-01 | 64980019001 | 100 TABLET in 1 BOTTLE, PLASTIC (64980-190-01) | 100 tablet | 2012-09-21 | 0000-00-00 | No | No | Current |
| 64980-190-03 | 64980019003 | 30 TABLET in 1 BOTTLE, PLASTIC (64980-190-03) | 30 tablet | 2012-09-21 | 0000-00-00 | No | No | Current |
| 64980-190-10 | 64980019010 | 1000 TABLET in 1 BOTTLE, PLASTIC (64980-190-10) | 1000 tablet | 2012-09-21 | 0000-00-00 | No | No | Current |