Penicillamine
- Product NDC
- 71205-916
- 11-digit product format
- 712050916
- Labeler code
- 71205
- Product ID
- 71205-916_125ca13e-9784-45be-847a-6fdf9875bd6a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Penicillamine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA211735
- Marketing category
- ANDA
- Marketing start
- 2020-12-21
- 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 | 198070 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71205-916-00 | Penicillamine | 100 in 1 BOTTLE | CAPSULE | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-916 | PENICILLAMINE CAPSULE [PROFICIENT RX LP] | 2 | Current NDC, Legacy NDC, 1 package rows | 20220420_c92335c6-f6fa-4768-9401-55c6b7f87699.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 |
|---|
| 71205-916-00 | 71205091600 | 100 CAPSULE in 1 BOTTLE (71205-916-00) | 100 capsule | 2021-07-08 | 0000-00-00 | No | No | Current |