AMPHETAMINE SULFATE
- Product NDC
- 0527-2525
- 11-digit product format
- 005272525
- Labeler code
- 0527
- Product ID
- 0527-2525_23880d0f-9eea-4ef3-95aa-10fc11fcfa6c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- amphetamine sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA212901
- Marketing category
- ANDA
- Marketing start
- 2020-05-25
- Substance
- AMPHETAMINE SULFATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- AMPHETAMINE SULFATE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AMPHETAMINE SULFATE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6DPV8NK46S |
| Rxcui | 884655, 1600695 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0527-2525-37 | AMPHETAMINE SULFATE | 100 in 1 BOTTLE | TABLET | 100 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0527-2525 | AMPHETAMINE SULFATE TABLET [LANNETT COMPANY, INC.] | 7 | Current NDC, Legacy NDC, 1 package rows | 20240123_85a015a7-a1a0-4b04-8bc4-7aacd0c84742.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0527-2525-37 | 00527252537 | 100 TABLET in 1 BOTTLE (0527-2525-37) | 100 tablet | 2020-06-01 | 0000-00-00 | No | No | Current |