Class III · Low risk
Hydrocodone Bitartrate and Homatropine Methlybromide tablets
Failed Impurities/Degradation Specifications
National Drug Code
Is NDC 10702-0055-03 recalled?
Hydrocodone Bitartrate and Homatropine Methylbromide · 30 TABLET in 1 BOTTLE (10702-055-03)
Yes — this exact package was recalled
1 FDA recall names the code 10702-0055-03 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Hydrocodone Bitartrate and Homatropine Methylbromide
- Strength
- HYDROCODONE BITARTRATE 5 mg/1; HOMATROPINE METHYLBROMIDE…
- Form
- Tablet · Oral
- Labeler
- KVK-Tech, Inc.
- Type
- Human Prescription Drug · DEA CII
- Product code
- 10702-0055
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 10702-0026 Phentermine Hydrochloride 3
- 10702-0028 Phentermine Hydrochloride 2
- 10702-0040 Benzphetamine Hydrochloride 2
- 10702-0052 See recall 2
- 10702-0010 Hydroxyzine Hydrochloride 1
- 10702-0011 Hydroxyzine Hydrochloride 1
Free recall alerts
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