Quinine Sulfate
- Product NDC
- 0093-3002
- 11-digit product format
- 000933002
- Labeler code
- 0093
- Product ID
- 0093-3002_29ebf3c2-8351-43c3-82ac-3b118fb7faf6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinine Sulfate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA091661
- Marketing category
- ANDA
- Marketing start
- 2012-09-28
- Substance
- QUININE SULFATE
- Active strength
- 324 mg/1
- Pharmacologic classes
- Antimalarial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Quinine Sulfate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| QUININE SULFATE | 324 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | KF7Z0E0Q2B |
| Rxcui | 997010 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0093-3002-56 | Quinine Sulfate | 30 in 1 BOTTLE | CAPSULE | 30 | | 13 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0093-3002 | QUININE SULFATE CAPSULE [TEVA PHARMACEUTICALS USA, INC.] | 10 | Current NDC, Legacy NDC, 1 package rows | 20230831_e782283e-2608-4fd6-a8b2-6c30b9d5d3b0.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 |
|---|
| 0093-3002-56 | 00093300256 | 30 CAPSULE in 1 BOTTLE (0093-3002-56) | 30 capsule | 2012-09-28 | 0000-00-00 | No | No | Current |