Penicillamine
- Product NDC
- 70748-153
- 11-digit product format
- 707480153
- Labeler code
- 70748
- Product ID
- 70748-153_99f3ca78-1663-47a1-9ed3-9c4eaa9f0271
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Penicillamine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA212933
- Marketing category
- ANDA
- Marketing start
- 2021-03-01
- Substance
- PENICILLAMINE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Antirheumatic Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Penicillamine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PENICILLAMINE | 250 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | GNN1DV99GX |
| Rxcui | 198071 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70748-153-01 | Penicillamine | 100 in 1 BOTTLE | TABLET | 100 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70748-153 | PENICILLAMINE TABLET [LUPIN PHARMACEUTICALS, INC.] | 6 | Current NDC, Legacy NDC, 1 package rows | 20230105_f6ecaf47-902f-4378-b524-7a88f20ba138.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 |
|---|
| 70748-153-01 | 70748015301 | 100 TABLET in 1 BOTTLE (70748-153-01) | 100 tablet | 2021-03-01 | 0000-00-00 | No | No | Current |