Amphetamine Sulfate
- Product NDC
- 72162-1612
- 11-digit product format
- 721621612
- Labeler code
- 72162
- Product ID
- 72162-1612_f5bd68ee-e949-4326-a7b6-091b313ade09
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amphetamine Sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA200166
- Marketing category
- ANDA
- Marketing start
- 2018-03-29
- Substance
- AMPHETAMINE SULFATE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Amphetamine Sulfate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AMPHETAMINE SULFATE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6DPV8NK46S |
| Rxcui | 884655 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1612-3 | Amphetamine Sulfate | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1612 | AMPHETAMINE SULFATE TABLET [BRYANT RANCH PREPACK] | 1 | Current NDC, 1 package rows | 20240702_920f99f4-ab78-4eed-9d80-08a2ebd0b769.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1612-3 | 72162161203 | 30 TABLET in 1 BOTTLE (72162-1612-3) | 30 tablet | 2021-01-07 | No | No | Historical |