Benzphetamine Hydrochloride
- Product NDC
- 75834-102
- 11-digit product format
- 758340102
- Labeler code
- 75834
- Product ID
- 75834-102_103b4cf1-4b5d-44b3-89e2-a393ef4f2276
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzphetamine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Nivagen Pharmaceuticals, Inc.
- Application
- ANDA040747
- Marketing category
- ANDA
- Marketing start
- 2016-01-15
- Marketing end
- 0000-00-00
- Substance
- BENZPHETAMINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]
- DEA schedule
- CIII
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 75834-102-01 | Benzphetamine Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 75834-102-05 | Benzphetamine Hydrochloride | 500 in 1 BOTTLE | TABLET | 500 | | 1 |
| 75834-102-30 | Benzphetamine Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75834-102 | BENZPHETAMINE HYDROCHLORIDE TABLET [NIVAGEN PHARMACEUTICALS, INC.] | 1 | Legacy NDC, 3 package rows | 20160127_5f5b95b3-a18f-4289-b9a6-a3278ef5966d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 75834-102-01 | 75834010201 | 100 in 1 BOTTLE | Historical |
| 75834-102-05 | 75834010205 | 500 in 1 BOTTLE | Historical |
| 75834-102-30 | 75834010230 | 30 in 1 BOTTLE | Historical |